Scalp defect, nipples absence and ears abnormalities: an other case of Finlay syndrome.
作者信息
Le Merrer M, Renier D, Briard M L
机构信息
Unité de Recherches sur les handicaps Génétiques de l'Enfant INSERM U12, Hôpital Necker-Enfants Malades.
出版信息
Genet Couns. 1991;2(4):233-6.
PMID:1799422
Abstract
Bilateral absence of nipples is an exceptional defect. We report the second family with the association of scalp defect, abnormally shaped ears and absence of nipples described by Finlay as an autosomal dominant trait.
摘要
Zotero 插件