NEUROFIBROMATOSIS - NEW CLINICAL AND GENETIC-ASPECTS

被引：0

作者：

FROSTERISKENIUS, UG ^{[1
]}

WOLFF, HH ^{[1
]}

机构：

[1] MED UNIV LUBECK,DERMATOL & VENEROL KLIN,W-2400 LUBECK 1,GERMANY

来源：

HAUTARZT | 1991年 / 42卷 / 05期

关键词：

NEUROFIBROMATOSIS; RECKLINGHAUSEN DISEASE; CLASSIFICATION; GENETICS;

D O I：

暂无

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Neurofibromatosis is not a single entity. Seven types of the disorder are now known, which can be differentiated by clinical and genetic features. The wide variety of clinical manifestations makes close interdisciplinary cooperation necessary, in which the dermatologist frequently has a key role. The most frequent forms are peripheral neurofibromatosis (NF1) and central neurofibromatosis (NF2), for which separate gene localizations have been found on chromosomes 17 and 22, respectively, by molecular genetics techniques. The meanwhile possible prenatal diagnosis raises ethical questions.

引用

页码：279 / 283

页数：5

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