Leopard syndrome

被引：7
|
作者：
Shamsadini, S [1 ]
Abazardi, H [1 ]
Shamsadini, F [1 ]
机构：
[1] Kerman Univ Med Sci, Kerman Darman Hosp, Kerman, Iran
来源：
LANCET | 1999年 / 354卷 / 9189期
关键词：
D O I：
10.1016/S0140-6736(99)03794-0
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
An 18-year-old girl with Leopard syndrome is described. Clinical manifestations include lentigines, ocular hypertelorism, mental and growth retardation, deafmuteness, and several patches of hair loss on her scalp. No family history of skin lentiginosis or any other inherited condition was found.
引用
收藏
页码：1530 / 1530
页数：1
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