Dentin dysplasia type I: a case report and review of the literature

Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp cham...
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Autor*in:	Toomarian, Lida [verfasserIn] Mashhadiabbas, Fatemeh Mirkarimi, Mahkameh Mehrdad, Leili

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2010

Schlagwörter:	Pulp Chamber Carious Tooth Dentin Formation Radicular Cyst Dentinogenesis Imperfecta

Anmerkung:	© Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (

Übergeordnetes Werk:	Enthalten in: Journal of medical case reports - London : BioMed Central, 2007, 4(2010), 1 vom: 07. Jan.
Übergeordnetes Werk:	volume:4 ; year:2010 ; number:1 ; day:07 ; month:01

Links:	Volltext

DOI / URN:	10.1186/1752-1947-4-1

Katalog-ID:	SPR03103778X

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520			\|a Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition.
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allfields	10.1186/1752-1947-4-1 doi (DE-627)SPR03103778X (SPR)1752-1947-4-1-e DE-627 ger DE-627 rakwb eng Toomarian, Lida verfasserin aut Dentin dysplasia type I: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. Pulp Chamber (dpeaa)DE-He213 Carious Tooth (dpeaa)DE-He213 Dentin Formation (dpeaa)DE-He213 Radicular Cyst (dpeaa)DE-He213 Dentinogenesis Imperfecta (dpeaa)DE-He213 Mashhadiabbas, Fatemeh aut Mirkarimi, Mahkameh aut Mehrdad, Leili aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 07. Jan. (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:07 month:01 https://dx.doi.org/10.1186/1752-1947-4-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 07 01
spelling	10.1186/1752-1947-4-1 doi (DE-627)SPR03103778X (SPR)1752-1947-4-1-e DE-627 ger DE-627 rakwb eng Toomarian, Lida verfasserin aut Dentin dysplasia type I: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. Pulp Chamber (dpeaa)DE-He213 Carious Tooth (dpeaa)DE-He213 Dentin Formation (dpeaa)DE-He213 Radicular Cyst (dpeaa)DE-He213 Dentinogenesis Imperfecta (dpeaa)DE-He213 Mashhadiabbas, Fatemeh aut Mirkarimi, Mahkameh aut Mehrdad, Leili aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 07. Jan. (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:07 month:01 https://dx.doi.org/10.1186/1752-1947-4-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 07 01
allfields_unstemmed	10.1186/1752-1947-4-1 doi (DE-627)SPR03103778X (SPR)1752-1947-4-1-e DE-627 ger DE-627 rakwb eng Toomarian, Lida verfasserin aut Dentin dysplasia type I: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. Pulp Chamber (dpeaa)DE-He213 Carious Tooth (dpeaa)DE-He213 Dentin Formation (dpeaa)DE-He213 Radicular Cyst (dpeaa)DE-He213 Dentinogenesis Imperfecta (dpeaa)DE-He213 Mashhadiabbas, Fatemeh aut Mirkarimi, Mahkameh aut Mehrdad, Leili aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 07. Jan. (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:07 month:01 https://dx.doi.org/10.1186/1752-1947-4-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 07 01
allfieldsGer	10.1186/1752-1947-4-1 doi (DE-627)SPR03103778X (SPR)1752-1947-4-1-e DE-627 ger DE-627 rakwb eng Toomarian, Lida verfasserin aut Dentin dysplasia type I: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. Pulp Chamber (dpeaa)DE-He213 Carious Tooth (dpeaa)DE-He213 Dentin Formation (dpeaa)DE-He213 Radicular Cyst (dpeaa)DE-He213 Dentinogenesis Imperfecta (dpeaa)DE-He213 Mashhadiabbas, Fatemeh aut Mirkarimi, Mahkameh aut Mehrdad, Leili aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 07. Jan. (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:07 month:01 https://dx.doi.org/10.1186/1752-1947-4-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 07 01
allfieldsSound	10.1186/1752-1947-4-1 doi (DE-627)SPR03103778X (SPR)1752-1947-4-1-e DE-627 ger DE-627 rakwb eng Toomarian, Lida verfasserin aut Dentin dysplasia type I: a case report and review of the literature 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. Pulp Chamber (dpeaa)DE-He213 Carious Tooth (dpeaa)DE-He213 Dentin Formation (dpeaa)DE-He213 Radicular Cyst (dpeaa)DE-He213 Dentinogenesis Imperfecta (dpeaa)DE-He213 Mashhadiabbas, Fatemeh aut Mirkarimi, Mahkameh aut Mehrdad, Leili aut Enthalten in Journal of medical case reports London : BioMed Central, 2007 4(2010), 1 vom: 07. Jan. (DE-627)524231389 (DE-600)2269805-X 1752-1947 nnns volume:4 year:2010 number:1 day:07 month:01 https://dx.doi.org/10.1186/1752-1947-4-1 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 4 2010 1 07 01
language	English
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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. 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topic_title	Dentin dysplasia type I: a case report and review of the literature Pulp Chamber (dpeaa)DE-He213 Carious Tooth (dpeaa)DE-He213 Dentin Formation (dpeaa)DE-He213 Radicular Cyst (dpeaa)DE-He213 Dentinogenesis Imperfecta (dpeaa)DE-He213
topic	misc Pulp Chamber misc Carious Tooth misc Dentin Formation misc Radicular Cyst misc Dentinogenesis Imperfecta
topic_unstemmed	misc Pulp Chamber misc Carious Tooth misc Dentin Formation misc Radicular Cyst misc Dentinogenesis Imperfecta
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title_auth	Dentin dysplasia type I: a case report and review of the literature
abstract	Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstractGer	Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
abstract_unstemmed	Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. Radiographic analysis shows obliteration of all pulp chambers, short, blunted and malformed or absent roots and peri-apical radiolucencies of non carious teeth. Case presentation We present a case of dentin dysplasia type I in a 12-year-old Iranian boy, and the clinical, radiographic and histopathologic findings of this condition and treatment are described. Conclusions There are still many inconclusive issues in the diagnosis and management of patients with dentin dysplasia. The diagnostic features of this rare disturbance will remain incompletely defined until additional cases have been described. Early diagnosis of the condition and initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition. © Toomarian et al; licensee BioMed Central Ltd. 2010. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (
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title_short	Dentin dysplasia type I: a case report and review of the literature
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