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[Brown-Vialleto-van Laere syndrome: report of 2 cases].

作者信息

De Oliveira J T, Moreira P R, Cardoso F, Perpétuo F O

机构信息

Serviço de Neurologia, Universidade Federal de Minas Gerais, Brasil.

出版信息

Arq Neuropsiquiatr. 1995 Dec;53(4):789-91. doi: 10.1590/s0004-282x1995000500013.

Abstract

Brown-Vialetto-van Laere syndrome is a rare hereditary or sporadic degenerative disorder characterised by progressive sensoryneural deafness, followed or accompanied by cranial nerve palsies. The anterior horn cells and the optic pathways may be involved in some cases. We report two cases, and comment the differential diagnosis and the relationships of this syndrome to the muscle spinal atrophies and the hereditary deafness.

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