Hereditary Motor and Sensory Neuropathy Type VI with Bilateral Middle Cerebellar Peduncle Involvement
Experimental Neurobiology
;
: 266-269, 2014.
Article
in English
| WPRIM
| ID: wpr-50919
ABSTRACT
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 mostly involved. We report a patient confirmed as HMSN VI who had isolated bilateral middle cerebellar peduncular lesions in brain MRI.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Brain
/
Magnetic Resonance Imaging
/
Hereditary Sensory and Motor Neuropathy
/
Charcot-Marie-Tooth Disease
/
Central Nervous System
/
Optic Atrophy
/
Mitochondria
Limits:
Humans
Language:
English
Journal:
Experimental Neurobiology
Year:
2014
Type:
Article
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