色素失禁症伴双侧唇腭裂。

Incontinentia pigmenti associated with bilateral cleft lip and palate.

作者信息

Yell J A, Walshe M, Desai S N

机构信息

Department of Dermatology, Stoke Mandeville Hospital, Aylesbury, Bucks, UK.

出版信息

Clin Exp Dermatol. 1991 Jan;16(1):49-50. doi: 10.1111/j.1365-2230.1991.tb00296.x.

DOI:10.1111/j.1365-2230.1991.tb00296.x

PMID:2025936

Abstract

Incontinentia pigmenti (Bloch-Sulzberger syndrome) is an uncommon genodermatosis mainly affecting females. It consists of characteristic skin manifestations associated in 79.8% of patients with other systemic manifestations. Of these there have been five cases of palatal or lip abnormalities, none being bilateral cleft lip and palate. We describe a unique case of incontinentia pigmenti associated with a bilateral cleft lip and palate.

摘要

色素失禁症（布洛赫-苏尔茨贝格综合征）是一种主要影响女性的罕见遗传性皮肤病。它由特征性皮肤表现组成，79.8%的患者伴有其他全身表现。其中有5例出现腭部或唇部异常，均非双侧唇腭裂。我们描述了1例与双侧唇腭裂相关的色素失禁症罕见病例。