ANGIOKERATOMA CORPORIS DIFFUSUM IN A PATIENT WITH NORMAL ENZYME-ACTIVITIES AND TURNERS SYNDROME

被引：15

作者：

GASPARINI, G ^{[1
]}

SARCHI, G ^{[1
]}

CAVICCHINI, S ^{[1
]}

BERTAGNOLIO, B ^{[1
]}

机构：

[1] IST C BESTA, BIOCHIM & GENET SISTEMA NERVOSO, MILAN, ITALY

来源：

CLINICAL AND EXPERIMENTAL DERMATOLOGY | 1992年 / 17卷 / 01期

关键词：

D O I：

10.1111/j.1365-2230.1992.tb02537.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

A case of angiokeratoma corporis diffusum (ACD) involving the skin of a 26-year-old patient with Turner's syndrome presenting with normal physical and mental development is reported. The unusual nature of this association confirms the theory that ACD presenting with skin lesions alone is a rare but specific clinical entity which differs from the hereditary sphingolipidoses like Fabry's disease.

引用

页码：56 / 59

页数：4

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