Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndrome.

We report on the occurrence of coronal craniosynostosis, anal anomalies, and porokeratosis in two male sibs. A third male sib was phenotypically normal as were the parents. The occurrence of these three clinical features has, to our knowledge, not been reported before. Cutaneous or anal anomalies or...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Flanagan, N, Boyadjiev, S A, Harper, J, Kyne, L, Earley, M, Watson, R, Jabs, E W, Geraghty, M T
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1998
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051430/
https://ncbi.nlm.nih.gov/pubmed/9733036
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