Gorlin–Goltz Syndrome with Multidisciplinary Approach of Treatment
Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma s...
Ausführliche Beschreibung
Autor*in: |
Jayachandran Sadaksharam [verfasserIn] Amutha Velappan Annapoorni [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2019 |
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Schlagwörter: |
multiple odontogenic keratocyst syndrome |
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Übergeordnetes Werk: |
In: Annals of the National Academy of Medical Sciences (India) - Thieme Medical and Scientific Publishers Pvt. Ltd., 2015, 55(2019), 04, Seite 213-218 |
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Übergeordnetes Werk: |
volume:55 ; year:2019 ; number:04 ; pages:213-218 |
Links: |
Link aufrufen |
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DOI / URN: |
10.1055/s-0039-3402665 |
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Katalog-ID: |
DOAJ018759939 |
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10.1055/s-0039-3402665 doi (DE-627)DOAJ018759939 (DE-599)DOAJ1e031f07551f451eb833142f3f5fc74a DE-627 ger DE-627 rakwb eng R5-130.5 Jayachandran Sadaksharam verfasserin aut Gorlin–Goltz Syndrome with Multidisciplinary Approach of Treatment 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This article illustrates about the clinical, radiological, and histological diagnostic findings and the multidisciplinary approach of treatment given to one such rare case of Gorlin–Goltz syndrome. gorlin–goltz syndrome multiple odontogenic keratocyst syndrome nevoid basal cell carcinoma syndrome gorlin’s syndrome General works Science Q Amutha Velappan Annapoorni verfasserin aut In Annals of the National Academy of Medical Sciences (India) Thieme Medical and Scientific Publishers Pvt. Ltd., 2015 55(2019), 04, Seite 213-218 (DE-627)1681809117 24545635 nnns volume:55 year:2019 number:04 pages:213-218 https://doi.org/10.1055/s-0039-3402665 kostenfrei https://doaj.org/article/1e031f07551f451eb833142f3f5fc74a kostenfrei http://www.thieme-connect.de/DOI/DOI?10.1055/s-0039-3402665 kostenfrei https://doaj.org/toc/0379-038X Journal toc kostenfrei https://doaj.org/toc/2454-5635 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_21 GBV_ILN_267 AR 55 2019 04 213-218 |
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Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This article illustrates about the clinical, radiological, and histological diagnostic findings and the multidisciplinary approach of treatment given to one such rare case of Gorlin–Goltz syndrome. |
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Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This article illustrates about the clinical, radiological, and histological diagnostic findings and the multidisciplinary approach of treatment given to one such rare case of Gorlin–Goltz syndrome. |
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Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This article illustrates about the clinical, radiological, and histological diagnostic findings and the multidisciplinary approach of treatment given to one such rare case of Gorlin–Goltz syndrome. |
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