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Crouzon's syndrome: A review of literature and case report

Crouzon's syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon's syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene. Normally, th...

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Bibliographic Details
Main Authors: Padmanabhan, Vivek, Hegde, Amitha M., Rai, Kavita
Format: Artigo
Language:Inglês
Published: Medknow Publications Pvt Ltd 2011
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3214529/
https://ncbi.nlm.nih.gov/pubmed/22215936
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.86464
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