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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Detaylı Bibliyografya
Asıl Yazarlar: Jawa, Deepti Singh, Sircar, Keya, Somani, Rani, Grover, Neeraj, Jaidka, Shipra, Singh, Sanjeet
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications 2009
Konular:
Case Report
Online Erişim: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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