Hereditary Motor and Sensory Neuropathy Type VI with Bilateral Middle Cerebellar Peduncle Involvement

Charcot-Marie-Tooth disease (CMT) 2A with optic atrophy is referred to as hereditary motor and sensory neuropathy type VI (HMSN VI) and is caused by mitofusin 2 gene (MFN2) mutation. In patients with MFN2 related CMT, central nervous system is known to be also involved and cerebral white matter is m...

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Bibliographic Details
Main Authors: Oh, Jung-Hwan, Lee, Han Sang, Cha, Dong Min, Kang, Sa-Yoon
Format: Artigo
Language:Inglês
Published: The Korean Society for Brain and Neural Science 2014
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4174619/
https://ncbi.nlm.nih.gov/pubmed/25258575
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5607/en.2014.23.3.266
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