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Results 1 - 10 of 16 for Skeletal muscle atrophy
  1. LMNA gene 
    ... dystrophy (L-CMD), a rare condition characterized by skeletal muscle weakness and atrophy beginning very early in life. Most of the ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics
  2. LAMA2 gene 
    ... dystrophy, a disorder that causes weakness and wasting (atrophy) of skeletal muscles. This condition generally appears in one of two ...
    https://medlineplus.gov/genetics/gene/lama2 - Genetics
  3. SMN1 gene 
    ... and wasting (atrophy) in muscles used for movement (skeletal muscles) that worsens with age. Spinal muscular atrophy has a wide range of severity. There are ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
  4. SMN2 gene 
    ... and wasting (atrophy) in muscles used for movement (skeletal muscles) that worsens with age. Spinal muscular atrophy has a wide range of severity. There are ...
    https://medlineplus.gov/genetics/gene/smn2 - Genetics
  5. FHL1 gene 
    ... T KYOT LIM protein SLIMMER MGC111107 RBMX1A RBMX1B skeletal muscle LIM-protein 1 SLIM SLIM-1 SLIM1 SLIMMER XMPMA ... DOMINANT; SPM MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMA REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, ...
    https://medlineplus.gov/genetics/gene/fhl1 - Genetics
  6. OPA1 gene 
    ... movement and sensation (motor and sensory neuropathy), and skeletal muscle weakness ... brain dysfunction (encephalopathy), loss of sensation and weakness ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  7. TRPV4 gene 
    ... spinal muscular atrophy, which involves weakness and wasting (atrophy) of muscles in the shoulders and lower legs.Most of the TRPV4 gene mutations that cause these skeletal and neurological disorders change single amino acids in ...
    https://medlineplus.gov/genetics/gene/trpv4 - Genetics
  8. CNBP gene 
    ... by a Myotonic Dystrophy Type 2 Gene Causes Muscle Atrophy. Mol Cell Biol. 2018 Jun 28;38(14): ...
    https://medlineplus.gov/genetics/gene/cnbp - Genetics
  9. FGFR3 gene 
    ... abnormality called seborrheic keratosis and in people with skeletal disorders known as thanatophoric dysplasia, Crouzon syndrome with ... acanthosis nigricans (SADDAN). However, in contrast to the skeletal conditions, the variants associated with epidermal nevi (and ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  10. DMD gene 
    ... is located primarily in muscles used for movement (skeletal muscles) and in heart (cardiac) muscle. Small amounts ... present in nerve cells in the brain.In skeletal and cardiac muscles, dystrophin is part of a ...
    https://medlineplus.gov/genetics/gene/dmd - Genetics
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