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Cornelia De-Lange Syndrome: A Case Report

Cornelia de-Lange syndrome is a congenital anomaly syndrome characterized by distinctive facial dysmorphism, primordial short stature, hirsutism, and upper limb reduction defects that range from subtle phalangeal abnormalities to oligodactyly. Craniofacial features include synophrys, arched eyebrows...

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Autori principali: Mehta, Diana Noshir, Bhatia, Rupinder
Natura: Artigo
Lingua:Inglês
Pubblicazione: Jaypee Brothers Medical Publishers 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4086580/
https://ncbi.nlm.nih.gov/pubmed/25206204
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5005/jp-journals-10005-1201
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