Familial Ectrodactyly Syndrome in a Nigerian Child: A Case Report

Ectrodactyly, also known as Split-Hand/Split-Foot Malformation (SHFM) is a rare genetic condition characterized by defects of the central elements of the autopod. It has a prevalence of 1:10,000-1:90,000 worldwide. The X-linked and autosomal dominant types have been described. It can occur as an iso...

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Detalhes bibliográficos
Main Authors: Durowaye, Mathew, Adeboye, Muhammed, Yahaya-Kongoila, Sefiyah, Adaje, Adeline, Adesiyun, Omotayo, Ernest, Samuel Kolade, Mokuolu, Olugbenga Ayodeji, Adegboye, Abdulrasheed
Formato: Artigo
Idioma:Inglês
Publicado em: OMJ 2011
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3191709/
https://ncbi.nlm.nih.gov/pubmed/22043435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5001/omj.2011.67
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