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Progressive distal muscular atrophy
- ... and symptoms of the condition. Hereditary myoclonus with progressive distal muscular atrophy Jankovic-Rivera syndrome SMA-PME SMAPME Genetic Testing Registry: Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Spinal muscular atrophy-progressive myoclonic ...
- ... this gene, the condition is also known as distal anoctaminopathy. Miyoshi myopathy is a muscle disorder that is characterized by progressive weakness and atrophy of muscles that are away from the center ...
- ... motor neurons). Damage to motor neurons leads to progressive weakness and loss of muscle tissue (atrophy) in the feet and legs. HSPB1 gene variants are the most common cause of distal hereditary motor neuropathy, type II. The HSPB1 gene ...
- ... is a muscle disorder that is characterized by progressive weakness and atrophy of muscles that are away from the center of the body (distal muscles), particularly those in the legs. The DYSF ...
- ... have been found to cause a condition called distal hereditary motor ... of muscle tissue (atrophy) in the feet and legs. Research suggests that ...
- ... to muscles away from the body's center (distal). The muscle weakness usually worsens ... myoclonic epilepsy, spinal muscular atrophy with lower extremity ...
- ... distal spinal muscular atrophy 1 DHMN6 Diaphragmatic spinal muscular atrophy Distal hereditary motor neuronopathy type VI Distal spinal muscular atrophy type 1 DSMA1 HMN6 HMNVI Severe infantile axonal ...
- ... occurs later and is less severe than the muscle atrophy in the lower legs. Some individuals with distal hereditary motor neuropathy, type II can also experience ...
- ... U, Schuetz A, Schuelke M. Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 ...
- ... gene damages or destroys these cells, leading to progressive muscle weakness and atrophy.The DUX4 gene is located next to a ...