Gorlin-Goltz syndrome: A rare case report

Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts (OKCs) and musculoskeletal malformations. A rare case of this syndrome observed in a 13-year-old male patient is presented in which multiple OKCs were c...

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Asıl Yazarlar: Chetan A Pol (Yazar), Suvarna K Ghige (Yazar), Ritesh R Kalaskar (Yazar), Suchitra R Gosavi (Yazar)
Materyal Türü: Kitap
Baskı/Yayın Bilgisi: Wolters Kluwer Medknow Publications, 2013-01-01T00:00:00Z.
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