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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.

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Pfeiffer, R A, Völklein, J
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1982
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048930/
https://ncbi.nlm.nih.gov/pubmed/7143396
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