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[棘层松解性表皮痣:棘层松解是遗传性的,而非痣]

[Acanthokeratolytic epidermal nevus: acanthokeratolysis is hereditary, not the nevus].

作者信息

Happle R

机构信息

Dermatologische Klinik, Universität Nijmegen.

出版信息

Hautarzt. 1990 Mar;41(3):117-8.

PMID:2188933
Abstract

Epidermal naevus of the acanthokeratolytic (epidermolytic) type is a mosaic birth defect. The underlying mutation may also be present in the gonads and can then be transmitted to the next generation. The affected child, however, will always show a diffuse involvement of the entire body in the form of bullous congenital ichthyosiform erythroderma. In other words, the phenotype can be transmitted, but not the mosaic. This explains why acanthokeratolytic epidermal naevus always affects the parent and never the child when it is observed in a family together with bullous congenital ichthyosiform erythroderma.

摘要

棘层松解(表皮松解)型表皮痣是一种嵌合型出生缺陷。潜在的突变也可能存在于性腺中,进而可遗传给下一代。然而,患病儿童总是会以大疱性先天性鱼鳞病样红皮病的形式全身弥漫受累。换句话说,表型可以遗传,但嵌合型不会。这就解释了为什么当在一个家族中同时观察到棘层松解型表皮痣和大疱性先天性鱼鳞病样红皮病时,总是父母患病而孩子不患病。

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