Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?

We report two sibs of Turkish descent with multiple congenital anomalies including severe microcephaly, hygroma colli, cystic renal dysplasia, and bilateral cutaneous syndactyly of toes IV-V. In addition, the second sib presented with bilateral fusion of the eyelids, a bicornuate uterus, and clitoro...

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Detalhes bibliográficos
Main Authors: Janssen, H, Schaap, C, Vandevijver, N, Moerman, P, de Die-Smulders, C E M, Fryns, J
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 1999
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734377/
https://ncbi.nlm.nih.gov/pubmed/10874639
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