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- W4280598328 abstract "GNE myopathy is a rare distal myopathy caused by mutations of the GNE gene. A few cases of GNE myopathy accompanied by neurogenic features of electrophysiology mimicking hereditary motor neuropathy were reported recently. We confirmed this feature and described the clinical phenotype and mutations of GNE myopathy in these rare cases.The absence of lower limb tendon reflexes, decreased compound muscle action potentials in lower leg motor nerves, and neurogenic pattern of electromyography suggested neuropathy in four patients. However, muscle pathology revealed a predominantly myogenic pattern. The follow-up electroneurography results implied that the compound motor action potential amplitudes deteriorated over time. Next-generation sequencing identified three novel variants of the GNE gene, c.2054T > C (p.Val685Ala), c.424G > A (p.Gly142Arg) and c.944T > C (p.Phe315Ser), as well as two hotspot mutations, c.115C > T(p.Arg39*) and c.620A > T(p.Asp207Val), in these patients. These novel mutations cosegregated with disease in the family.These rare cases supported the existence of neurogenic features of electrophysiology different from the typical myopathic pattern of GNE myopathy." @default.
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- W4280598328 date "2022-05-19" @default.
- W4280598328 modified "2023-09-30" @default.
- W4280598328 title "Different electrophysiology patterns in GNE myopathy" @default.
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- W4280598328 doi "https://doi.org/10.1186/s13023-022-02355-0" @default.
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