Delayed diagnosis of Gorlin syndrome: Learning from mistakes!

Gorlin syndrome (GS) is a rare inherited multisystem disorder with predisposition to basal cell carcinomas and various other neoplasms. Characteristic features include falx calcification, multiple odontogenic keratocysts (OKCs), early onset medulloblastoma, craniofacial and skeletal malformations, c...

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Detaylı Bibliyografya
Yayımlandı:J Pediatr Neurosci
Asıl Yazarlar: Ramanathan, Subramaniyan, Kumar, Devendra, Al Heidous, Mahmoud, Palaniappan, Yegu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2015
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4770649/
https://ncbi.nlm.nih.gov/pubmed/26962343
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.174437
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