期刊文献+
共找到1篇文章
< 1 >
每页显示 20 50 100
先天性鱼鳞癣样红皮病患者SPINK5的突变:分子检测是诊断内瑟顿综合征(伴有结节毛的鱼鳞癣)的有效工具
1
作者 Sprecher E. tesfaye-kedjela a. +1 位作者 Ratajczak P. 马慧群 《世界核心医学期刊文摘(皮肤病学分册)》 2005年第2期34-34,共1页
The congenital erythrodermas represent a heterogeneous group of inherited and acquired disorders often accompanied by systemic infections, impaired epidermal barrier function and concomitant life-threatening fluid and... The congenital erythrodermas represent a heterogeneous group of inherited and acquired disorders often accompanied by systemic infections, impaired epidermal barrier function and concomitant life-threatening fluid and electrolyte imbalance. In the present report, we describe a patient who was considered to have congenital ichthyosiform erythroderma for 26 years until molecular testing led to the correct diagnosis of Netherton syndrome. 展开更多
关键词 鱼鳞癣 SPINK5 红皮病 分子检测 屏障功能 文章报道 电解质失衡
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部