Atypical presentation of GNE myopathy with asymmetric hand weakness.
Ontology highlight
ABSTRACT: GNE myopathy is a rare autosomal recessive muscle disease caused by mutations in GNE, the gene encoding the rate-limiting enzyme in sialic acid biosynthesis. GNE myopathy usually manifests in early adulthood with distal myopathy that progresses slowly and symmetrically, first involving distal muscles of the lower extremities, followed by proximal muscles with relative sparing of the quadriceps. Upper extremities are typically affected later in the disease. We report a patient with GNE myopathy who presented with asymmetric hand weakness. He had considerably decreased left grip strength, atrophy of the left anterior forearm and fibro-fatty tissue replacement of left forearm flexor muscles on T1-weighted magnetic resonance imaging. The patient was an endoscopist and thus the asymmetric hand
SUBMITTER: de Dios JK
PROVIDER: S-EPMC4259851 | biostudies-literature | 2014 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA