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Results 1 - 10 of 21 for Progressive distal muscular atrophy
  1. Spinal muscular atrophy with progressive myoclonic epilepsy 
    ... 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 ...
    https://medlineplus.gov/...rophy-with-progressive-myoclonic-epilepsy - Genetics
  2. ANO5 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/ano5 - Genetics
  3. DYSF 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 ...
    https://medlineplus.gov/genetics/gene/dysf - Genetics
  4. Spinal muscular atrophy 
    ... to muscles away from the body's center (distal). The muscle weakness usually worsens ... myoclonic epilepsy, spinal muscular atrophy with lower extremity ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  5. Distal hereditary motor neuropathy, type V 
    ... muscular atrophy, type V DSMAV HMN V Spinal muscular atrophy, distal type V Spinal muscular atrophy, distal, with upper limb predominance Genetic Testing Registry: Neuronopathy, ...
    https://medlineplus.gov/...distal-hereditary-motor-neuropathy-type-v - Genetics
  6. Spinal muscular atrophy with respiratory distress type 1 
    ... 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 ...
    https://medlineplus.gov/...-atrophy-with-respiratory-distress-type-1 - Genetics
  7. Distal hereditary motor neuropathy, type II 
    Distal hereditary motor neuropathy, type II is a progressive disorder that affects nerve cells in the spinal cord. It results in muscle weakness and affects movement, primarily in the legs.Onset of distal hereditary motor neuropathy, type II ranges from the ...
    https://medlineplus.gov/...istal-hereditary-motor-neuropathy-type-ii - Genetics
  8. IGHMBP2 gene 
    ... U, Schuetz A, Schuelke M. Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 ...
    https://medlineplus.gov/genetics/gene/ighmbp2 - Genetics
  9. Chromosome 4 
    ... gene damages or destroys these cells, leading to progressive muscle weakness and atrophy.The DUX4 gene is located next to a ...
    https://medlineplus.gov/genetics/chromosome/4 - Genetics
  10. DCTN1 gene 
    ... Finnegan K, Holzbaur EL, Fischbeck KH, Ludlow CL. Distal spinal and bulbar muscular atrophy caused by dynactin mutation. Ann Neurol. 2005 May; ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
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