Gorlin-Goltz syndrome

Gorlin-Goltz syndrome is a rare multisystemic disease inherited in an autosomal dominant pattern. It is characterized by numerous basal cell carcinoma of the skin, jaw cysts, and skeletal anomalies such as frontal bossing, vertebral anomalies, palmoplantar pits, and falx cerebri calcification. There...

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Dades bibliogràfiques
Publicat a:Turk Pediatri Ars
Autors principals: Şereflican, Betül, Tuman, Bengü, Şereflican, Murat, Halıcıoğlu, Sıddıka, Özyalvaçlı, Gülzade, Bayrak, Seval
Format: Artigo
Idioma:Inglês
Publicat: Turkish Pediatrics Association 2017
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5644586/
https://ncbi.nlm.nih.gov/pubmed/29062253
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/TurkPediatriArs.2017.2992
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