Gorlin-Goltz syndrome

Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder, which is characterized by multiple odontogenic Keratocysts and basal cell carcinomas, skeletal, dental, ophthalmic, and neurological abnormalities, intracranial ectopic calcifications of the falx cerebri, and facial dysmorph...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Joshi, Priya Shirish, Deshmukh, Vijay, Golgire, Someshwar
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2012
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3283966/
https://ncbi.nlm.nih.gov/pubmed/22363371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1735-3327.92963
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