Premature Craniosynostosis in a Rare Genetic Disease- A Case Report

Background: Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity. Its most notable characteristic feature is premature synostosis of cranial sutures The case presented is of a 4 yr old boy with box like head with micr...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Iran J Public Health
Egile Nagusiak: DHARAMSHI, Hasnain abbas, RAZA, Tufail, MOHSIN ALI, Ali Abbas, LILANI, Zuhair, AHSAN, Syed Zohaib, FARAZ, Ahmad, NAQVI, Syeda Tahira
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Tehran University of Medical Sciences 2015
Gaiak:
Case Report
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4402420/
https://ncbi.nlm.nih.gov/pubmed/25905085
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