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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Bibliographic Details
Main Authors: Jawa, Deepti Singh, Sircar, Keya, Somani, Rani, Grover, Neeraj, Jaidka, Shipra, Singh, Sanjeet
Format: Artigo
Language:Inglês
Published: Medknow Publications 2009
Subjects:
Case Report
Online Access: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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