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Congenital universal alopecia, mental deficiency, and microcephaly in two sibs
A brother and sister are reported who had congenital universal atrichosis, microcephaly, and mental retardation. Similar observations representing a rare nosological group are summarised. Heterogeneity is suggested. The pathogenesis of the individual syndromes is unknown.
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| Auteurs principaux: | , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
1982
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1048930/ https://ncbi.nlm.nih.gov/pubmed/7143396 |
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