Prosthodontic management of children with ectodermal dysplasia: A literature review
Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal f...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Abdulaziz. A. Alowairdhi [verfasserIn] |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2019 |
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| Übergeordnetes Werk: |
In: Saudi Dental Journal - Elsevier, 2007, 31(2019), Seite S70-S71 |
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| Übergeordnetes Werk: |
volume:31 ; year:2019 ; pages:S70-S71 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.sdentj.2019.02.036 |
|---|
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DOAJ010476296 |
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| 520 | |a Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. | ||
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10.1016/j.sdentj.2019.02.036 doi (DE-627)DOAJ010476296 (DE-599)DOAJ0cc7d7bb3d7a4de4a53523daddc3aaa9 DE-627 ger DE-627 rakwb eng RK1-715 Abdulaziz. A. Alowairdhi verfasserin aut Prosthodontic management of children with ectodermal dysplasia: A literature review 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. Medicine R Dentistry In Saudi Dental Journal Elsevier, 2007 31(2019), Seite S70-S71 (DE-627)608940313 (DE-600)2514342-6 16583558 nnns volume:31 year:2019 pages:S70-S71 https://doi.org/10.1016/j.sdentj.2019.02.036 kostenfrei https://doaj.org/article/0cc7d7bb3d7a4de4a53523daddc3aaa9 kostenfrei http://www.sciencedirect.com/science/article/pii/S1013905219301658 kostenfrei https://doaj.org/toc/1013-9052 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 31 2019 S70-S71 |
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10.1016/j.sdentj.2019.02.036 doi (DE-627)DOAJ010476296 (DE-599)DOAJ0cc7d7bb3d7a4de4a53523daddc3aaa9 DE-627 ger DE-627 rakwb eng RK1-715 Abdulaziz. A. Alowairdhi verfasserin aut Prosthodontic management of children with ectodermal dysplasia: A literature review 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. Medicine R Dentistry In Saudi Dental Journal Elsevier, 2007 31(2019), Seite S70-S71 (DE-627)608940313 (DE-600)2514342-6 16583558 nnns volume:31 year:2019 pages:S70-S71 https://doi.org/10.1016/j.sdentj.2019.02.036 kostenfrei https://doaj.org/article/0cc7d7bb3d7a4de4a53523daddc3aaa9 kostenfrei http://www.sciencedirect.com/science/article/pii/S1013905219301658 kostenfrei https://doaj.org/toc/1013-9052 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 31 2019 S70-S71 |
| allfields_unstemmed |
10.1016/j.sdentj.2019.02.036 doi (DE-627)DOAJ010476296 (DE-599)DOAJ0cc7d7bb3d7a4de4a53523daddc3aaa9 DE-627 ger DE-627 rakwb eng RK1-715 Abdulaziz. A. Alowairdhi verfasserin aut Prosthodontic management of children with ectodermal dysplasia: A literature review 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. Medicine R Dentistry In Saudi Dental Journal Elsevier, 2007 31(2019), Seite S70-S71 (DE-627)608940313 (DE-600)2514342-6 16583558 nnns volume:31 year:2019 pages:S70-S71 https://doi.org/10.1016/j.sdentj.2019.02.036 kostenfrei https://doaj.org/article/0cc7d7bb3d7a4de4a53523daddc3aaa9 kostenfrei http://www.sciencedirect.com/science/article/pii/S1013905219301658 kostenfrei https://doaj.org/toc/1013-9052 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 31 2019 S70-S71 |
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10.1016/j.sdentj.2019.02.036 doi (DE-627)DOAJ010476296 (DE-599)DOAJ0cc7d7bb3d7a4de4a53523daddc3aaa9 DE-627 ger DE-627 rakwb eng RK1-715 Abdulaziz. A. Alowairdhi verfasserin aut Prosthodontic management of children with ectodermal dysplasia: A literature review 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. Medicine R Dentistry In Saudi Dental Journal Elsevier, 2007 31(2019), Seite S70-S71 (DE-627)608940313 (DE-600)2514342-6 16583558 nnns volume:31 year:2019 pages:S70-S71 https://doi.org/10.1016/j.sdentj.2019.02.036 kostenfrei https://doaj.org/article/0cc7d7bb3d7a4de4a53523daddc3aaa9 kostenfrei http://www.sciencedirect.com/science/article/pii/S1013905219301658 kostenfrei https://doaj.org/toc/1013-9052 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 31 2019 S70-S71 |
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10.1016/j.sdentj.2019.02.036 doi (DE-627)DOAJ010476296 (DE-599)DOAJ0cc7d7bb3d7a4de4a53523daddc3aaa9 DE-627 ger DE-627 rakwb eng RK1-715 Abdulaziz. A. Alowairdhi verfasserin aut Prosthodontic management of children with ectodermal dysplasia: A literature review 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. Medicine R Dentistry In Saudi Dental Journal Elsevier, 2007 31(2019), Seite S70-S71 (DE-627)608940313 (DE-600)2514342-6 16583558 nnns volume:31 year:2019 pages:S70-S71 https://doi.org/10.1016/j.sdentj.2019.02.036 kostenfrei https://doaj.org/article/0cc7d7bb3d7a4de4a53523daddc3aaa9 kostenfrei http://www.sciencedirect.com/science/article/pii/S1013905219301658 kostenfrei https://doaj.org/toc/1013-9052 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 31 2019 S70-S71 |
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The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. 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Prosthodontic management of children with ectodermal dysplasia: A literature review |
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Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. |
| abstractGer |
Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. |
| abstract_unstemmed |
Introduction: Ectodermal dysplasia (ED) is a large group of heterogeneous heritable conditions characterized by congenital defects of two or more ectodermal structures and their appendages. The diagnosis of ED in early infancy period may be difficult in that sparse hair and absent teeth are normal findings at this stage of development. However, characteristic deformities of the skull including the square aspect of the forehead; frontal bossing; sunken cheeks; hyperpigmentation of the periorbital skin; prominent supraorbital ridges; saddle nose; and hypoplastic-appearing alaque nasi helps in diagnosing ED cases. In addition to its other symptoms, the dental characteristics of this syndrome include number anomalies such as anodontia or severe hypodontia (with or without a cleft lip and palate) that is associated with lack of alveolar ridge development and reduced vertical dimension. Clinically there are two major types of ED namely hidrotic and anhidrotic (hypohidrotic form). The hypohidrotic form is most common type with an incidence estimated to be 1–7 per 10,000 live births. The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. However, implants provide the best long term results and prognosis. |
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The goals of dental treatment for individuals affected by the ED syndromes are to provide an age-appropriate dentition that optimizes function, facial development, speech and esthetics. Dental management of children with ectodermal dysplasia includes removable, fixed and implant prosthesis. Materials and Method: A computerized search of the literature was done by searching the web based databases PubMed, Up To Date and the University of Texas Health Science Center for Critically Appraised Topics (CATS) library for key words including: Ectodermal Dysplasia, Prosthodontic Management of Ectodermal Dysplasia, Oral Manifestations of Ectodermal Dysplasia and Fixed and Removable Prosthodontic Management of Ectodermal Dysplasia. Titles and abstracts of the studies were evaluated according to relevance after obtaining the full text articles. The search ended in January 2017. The inclusion criteria were: studies that evaluated different modalities of treatment of ectodermal dysplasia, studies that addressed the effects of ectodermal dysplasia on oral health, reviews that addressed the clinical consequences of ectodermal dysplasia, case reports and case series of ectodermal dysplasia. Exclusion criteria: studies that were directed or focused to other aspects of ectodermal dysplasia other than oral health. Results: These patients often need a multidisciplinary approach to treatment planning and dental treatment to regain esthetics and function of the stomatognathic system. Considering the age, different rehabilitation options can be considered, from classic conventional solutions such as complete denture, removable partial denture, overdentures and to the most up to date implant supported prosthetics. Conclusion: Recall every 6 months with possible relining, rebasing or making a new denture. Following growth completion and occlusion stabilization an implant retained removable or fixed denture can be used to replace the missing teeth permanently. Moreover, traditional removable denture can be an option for replacing the missing teeth. 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