FAMILIAL SYSTEMATIZED EPIDERMAL NEVUS SYNDROME

被引:6
作者
MESCHIA, JF
JUNKINS, E
HOFMAN, KJ
机构
[1] JOHNS HOPKINS UNIV,SCH MED,CTR MED GENET,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21205
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1992年 / 44卷 / 05期
关键词
EPIDERMAL NEVUS; BLASCHKOS LINES; ICHTHYOSIS-HYSTRIX; HEMANGIOMA; HEMANGIOENDOTHELIOMA; SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; NEVUS-UNIUS-LATERIS; NEVUS-SEBACEOUS OF JADASSOHN;
D O I
10.1002/ajmg.1320440527
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Epidermal nevi are typically congenital but rarely familial. We report on a family in which 3 relatives have systematized epidermal nevi. The propositus also has evidence of a hemangioma and a hemangioendothelioma. Peripheral blood and skin fibroblast karyotypes of the propositus did not show evidence of mosaicism. Epidermal nevi have been associated with nondermatologic pathology, involving the nervous, vascular, and skeletal systems in sporadic cases. This report demonstrates that nondermatologic pathology can be also be associated with systematized epidermal nevi in a familial setting. The apparent skipping of generations may be explained by autosomal dominant inheritance with decreased penetrance.
引用
收藏
页码:664 / 667
页数:4
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