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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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| Pubblicato in: | J Med Genet |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMJ Publishing Group
1990
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| Soggetti: | |
| Accesso online: | 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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