Hutchinson-Gilford progeria syndrome

被引：7

作者：

Agarwal, Uma Shankar ^{[1
]}

Sitaraman, S. ^{[2
]}

Mehta, Sharad ^{[1
]}

Panse, Gauri ^{[1
]}

机构：

[1] SMS Med Coll & Hosp, Dept Dermatol, Jaipur, Rajasthan, India

[2] SMS Med Coll & Hosp, Dept Pediat, Jaipur, Rajasthan, India

来源：

INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY | 2010年 / 76卷 / 05期

关键词：

Hutchinson-Gilford syndrome; premature aging; progeria;

D O I：

10.4103/0378-6323.69094

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Progeria is a rare genetic disorder characterized by premature aging, involving the skin, bones, heart, and blood vessels. We report a 4-year-old boy who presented with clinical manifestations of progeria. He had characteristic facies, prominent eyes, scalp and leg veins, senile look, loss of scalp hair, eyebrows and eyelashes, stunted growth, and sclerodermatous changes. The present case is reported due to its rarity.

引用

页数：3

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