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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...

詳細記述

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書誌詳細
主要な著者: Flanagan, N, Boyadjiev, S A, Harper, J, Kyne, L, Earley, M, Watson, R, Jabs, E W, Geraghty, M T
フォーマット: Artigo
言語:Inglês
出版事項: 1998
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051430/
https://ncbi.nlm.nih.gov/pubmed/9733036
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