The acrocallosal syndrome in a Turkish boy.

A 6 month old Turkish boy with the acrocallosal syndrome is reported. The patient, born to consanguineous, healthy parents, presented with macrocephaly, a prominent forehead, hypertelorism, polydactyly of the fingers and toes, severe motor and mental retardation, hypotonia, and absence of the corpus...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:J Med Genet
Main Authors: Yüksel, M, Caliskan, M, Oğur, G, Ozmen, M, Dolunay, G, Apak, S
Format: Artigo
Jezik:Inglês
Izdano: BMJ Publishing Group 1990
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016880/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2308155/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.1.48
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