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Gorlin-Goltz syndrome

Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by the presence of multiple odontogenic keratocysts along with various cutaneous, dental, osseous, ophthalmic, neurological, and sex organ abnormalities. Early diagnosis is essential as it may progress to aggressive basa...

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Библиографические подробности
Главные авторы: Jawa, Deepti Singh, Sircar, Keya, Somani, Rani, Grover, Neeraj, Jaidka, Shipra, Singh, Sanjeet
Формат: Artigo
Язык:Inglês
Опубликовано: Medknow Publications 2009
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3162868/
https://ncbi.nlm.nih.gov/pubmed/21887009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0973-029X.57677
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