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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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Podrobná bibliografie
Hlavní autoři: Jawa, Deepti Singh, Sircar, Keya, Somani, Rani, Grover, Neeraj, Jaidka, Shipra, Singh, Sanjeet
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications 2009
Témata:
On-line přístup: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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