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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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| Main Authors: | , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
OMJ
2011
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| Fag: | |
| Online adgang: | 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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