Cutis Laxa syndrome: a case report

被引：7

作者：

Hbibi, Mohamed ^{[1
]}

Abourazzak, Sana ^{[1
]}

Idrissi, Mounia ^{[1
]}

Chaouki, Sana ^{[1
]}

Atmani, Samir ^{[1
]}

Hida, Moustapha ^{[1
]}

机构：

[1] Univ Hosp Hassan II Fes, Dept Pediat, Fes, Morocco

来源：

PAN AFRICAN MEDICAL JOURNAL | 2015年 / 20卷

关键词：

Cutis laxa; connective tissue; emphysema;

D O I：

10.11604/pamj.2015.20.3.5878

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal recessive and x-linked recessive patterns have been described in the inherited forms. Acquired forms of this disease have been associated with a previous inflammatory skin disorder (urticaria ...). The characteristic symptomatological pattern is resulting from paucity of elastic fibers. We report an 18 months old baby boy with a congenital cutis laxa. He was admitted in pediatric unit for respiratory disorders. The diagnosis of CL syndrome is based on clinical assessment of typical skin features and the associated extracutaneous finding.

引用

页数：4

共 8 条

[1] Autosomal recessive form of congenital cutis laxa:: More than the clinical appearance [J].