Chronic infantile neurological, cutaneous, and articular syndrome with severe early articular manifestations

被引：4

作者：

Leys, C

Eschard, C

Motte, J

Prieur, AM

Kalis, B

Bernard, P

机构：

[1] Univ Hosp, Dept Dermatol, Reims, France

[2] Univ Hosp, Dept Pediat, Reims, France

[3] Univ Hosp Necker, Dept Immunol, Paris, France

来源：

PEDIATRIC DERMATOLOGY | 2005年 / 22卷 / 03期

关键词：

D O I：

10.1111/j.1525-1470.2005.22316.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

We report an 11-month-old boy of French origin who had chronic, infantile, neurological, cutaneous, and articular syndrome with a particularly severe joint involvement with early onset. The diagnosis was based on the association of neurologic, cutaneous (urticarial skin eruption), and articular manifestations accompanied by recurrent bouts of fever. No mutation of the CIAS1 gene could be identified. Skeletal involvement was particularly severe, leading to considerable limitation of motion.

引用

页码：222 / 226

页数：5

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