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...

Full description

Saved in:
Bibliographic Details
Published in:J Pediatr Neurosci
Main Authors: Ramanathan, Subramaniyan, Kumar, Devendra, Al Heidous, Mahmoud, Palaniappan, Yegu
Format: Artigo
Language:Inglês
Published: Medknow Publications & Media Pvt Ltd 2015
Subjects:
Case Report
Online Access: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
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items