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...

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Detalles Bibliográficos
Autores principales: DHARAMSHI, Hasnain abbas, RAZA, Tufail, MOHSIN ALI, Ali Abbas, LILANI, Zuhair, AHSAN, Syed Zohaib, FARAZ, Ahmad, NAQVI, Syeda Tahira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402420/
https://www.ncbi.nlm.nih.gov/pubmed/25905085

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402420/
https://www.ncbi.nlm.nih.gov/pubmed/25905085

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