Common Genodermatoses: What the Pediatrician Needs to Know

被引：1
|
作者：
Mann, Julianne A. [1 ]
Siegel, Dawn H. [1 ]
机构：
[1] Oregon Hlth & Sci Univ, Dept Dermatol, Portland, OR 97239 USA
来源：
PEDIATRIC ANNALS | 2009年 / 38卷 / 02期
关键词：
TUBEROUS SCLEROSIS; INCONTINENTIA-PIGMENTI; MOUSE MODEL; NEUROFIBROMATOSIS TYPE-1; LASER TREATMENT; CHILDREN; MUTATION; DEFICITS; GENE; PREVALENCE;
D O I：
10.3928/00904481-20090201-08
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Recognizing the patterns of the skin findings and establishing the correct diagnosis can also help avoid subjecting patients to unnecessary tests, such as lumbar punctures to rule out herpes simplex virus in neonates with a Blaschkoid distribution of vesicles in incontinentia pigmenti. The cutaneous features of genetic disorders provide important clues to the underlying diagnoses for conditions such as tuberous sclerosis, neurofibromatosis, incontinentia pigmenti, and help direct the diagnostic evaluation and health supervision in those individuals.
引用
收藏
页码：91 / 98
页数：8
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