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Apert Syndrome: A Case Report

Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, midfacial malformation and symmetrical syndactyly. We present a 10-month-old infant having all the features of classical Apert syndrome. How to cite this article: Khan S, Chatra L, Shenai P, Veena...

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Detalles Bibliográficos
Autores principales: Khan, Saba, Chatra, Laxmikanth, Shenai, Prashanth, Veena, KM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155880/
https://www.ncbi.nlm.nih.gov/pubmed/25206168
http://dx.doi.org/10.5005/jp-journals-10005-1166

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