Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report

Split hand/foot malformation (SHFM) or ectrodactyly is a rare genetic condition affecting limb development. SHFM shows clinical and genetic heterogeneity. It can present as an isolated form or in combination with additional anomalies affecting the long bones (nonsyndromic form) or other organ system...

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Bibliografiset tiedot
Julkaisussa:Mol Syndromol
Päätekijät: Sivasankaran, Aswini, Srikanth, Ambika, Kulshreshtha, Pooja S., Anuradha, Deenadayalu, Kadandale, Jayarama S., Samuel, Chandra R.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: S. Karger AG 2016
Aiheet:
Novel Insights from Clinical Practice
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4802982/
https://ncbi.nlm.nih.gov/pubmed/27022330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000443708
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