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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.

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。

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引用本文的文献

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A case of incontinentia pigmenti associated with multiorgan abnormalities.
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