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Teaching NeuroImages: Hypertrophic olivary degeneration in a young man with POLGgene mutation

Authors :
Arkadir, David
Meiner, Vardiella
Karni, Arnon
Lossos, Alexander
Source :
Neurology (Ovid); February 2015, Vol. 84 Issue: 8 pe59-e59, 1p
Publication Year :
2015

Abstract

A 30-year-old man with sensorineural hearing loss presented with subacute somnolence, slurred speech, and unsteady gait following treatment with peginterferon α-2b and ribavirin for chronic hepatitis C virus. Examination revealed scanning speech, horizontal nystagmus, gait ataxia, and symmetric hyporeflexia with distal sensory loss. There was no palatal myoclonus. Metabolic and serologic workup and blood lactate were unrevealing. Brain MRI demonstrated bilateral hypertrophic olivary degeneration (HOD, figure). Whole exome sequencing identified a homozygous pathogenic p.W748S POLGmutation.1Differential diagnosis of bilateral HOD includes mutations in the nuclear genes crucial to mitochondrial function, POLGand SURF1.2

Details

Language :
English
ISSN :
00283878 and 1526632X
Volume :
84
Issue :
8
Database :
Supplemental Index
Journal :
Neurology (Ovid)
Publication Type :
Periodical
Accession number :
ejs49013154
Full Text :
https://doi.org/10.1212/WNL.0000000000001287