Inclusion Body Myopathy 2

Also known as Hereditary Inclusion Body Myopathy, GNE Myopathy

A condition characterized by slowly progressive muscle weakness in the lower legs and arms. Onset usually in the 20s. Symptoms vary and may result in being wheelchair-bound by about age 40 or having milder weakness, presenting later in life. Possible impact on lifespan. Physical impairment.

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