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Case Reports
, 13 (10), 830-4

A Novel Homozygous Missense Mutation in the GNE Gene of a Patient With Quadriceps-Sparing Hereditary Inclusion Body Myopathy Associated With Muscle Inflammation

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Case Reports

A Novel Homozygous Missense Mutation in the GNE Gene of a Patient With Quadriceps-Sparing Hereditary Inclusion Body Myopathy Associated With Muscle Inflammation

Sabine Krause et al. Neuromuscul Disord.

Abstract

An adult-onset hereditary inclusion body myopathy with sparing of the quadriceps muscle was originally described in Iranian Jews and assigned to a locus on chromosome 9p12-p13. Recently, mutations of the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (GNE) gene were reported to cause hereditary inclusion body myopathy and one type of distal myopathy in a world-wide distribution. Importantly, the lack of muscle inflammation was used to distinguish hereditary inclusion body myopathy from the sporadic form of inclusion body myopathy. We report a case of a quadriceps-sparing myopathy in a non-Jewish, Iranian patient with a high degree of muscle inflammation. A novel homozygous G-to-A mutation (128933G-->A) in exon 7 changing a valine to isoleucine (V367I) in the epimerase domain of the GNE gene was found. We conclude that muscle inflammation is not sufficient to exclude the diagnosis of hereditary inclusion body myopathy.

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