Lataa...
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:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
1982
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1048930/ https://ncbi.nlm.nih.gov/pubmed/7143396 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|