Neurological manifestations of neurofibromatosis: a review

被引：14

作者：

Bayat, Michael ^{[1
,2
]}

Bayat, Allan ^{[3
]}

机构：

[1] Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark

[2] Aarhus Univ Hosp, Ctr Rare Dis, Aarhus, Denmark

[3] Danish Epilepsy Ctr, Dianalund, Denmark

来源：

NEUROLOGICAL SCIENCES | 2020年 / 41卷 / 10期

关键词：

Neurofibromatosis; Neuropathy; Cerebrovascular disorders; Epilepsy; Neoplasms; Headache; UNIDENTIFIED BRIGHT OBJECTS; CENTRAL-NERVOUS-SYSTEM; CLINICAL PRESENTATION; CNS TUMORS; TYPE-1; CHILDREN; EPILEPSY; GLIOMAS; INDIVIDUALS; PREVALENCE;

D O I：

10.1007/s10072-020-04400-x

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Neurofibromatosis type 1(NF1) is a dominantly inherited genetic disorder caused by a mutation in the NF1 tumor-suppressor gene. Patients are prone to develop benign and malignant tumors not only in the central and peripheral nervous system but also in other parts of the body. Apart from tumors, neurofibromatosis may also be associated with neurological symptoms and disorders such as cerebrovascular disease, epilepsy, neuropathy, and headache. This article seeks to review the different neurological manifestations of neurofibromatosis.

引用

页码：2685 / 2690

页数：6

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