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Results 1 - 10 of 632 for muscles
  1. Congenital fibrosis of the extraocular muscles 
    Congenital fibrosis of the extraocular muscles (CFEOM) is a disorder of the nervous system that affects use of the muscles that surround the eyes (extraocular muscles). ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics
  2. Rippling muscle disease 
    Rippling muscle disease is a condition in which the muscles are unusually sensitive to movement or pressure (irritable). The muscles near the center of the body ( ...
    https://medlineplus.gov/genetics/condition/rippling-muscle-disease - Genetics
  3. Myostatin-related muscle hypertrophy 
    Myostatin-related muscle hypertrophy is a rare condition characterized by reduced body fat and increased muscle size. Affected individuals have up ...
    https://medlineplus.gov/.../myostatin-related-muscle-hypertrophy - Genetics
  4. Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome 
    Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps (HANAC) syndrome is part of a group of conditions called the COL4A1-related disorders. The conditions ...
    https://medlineplus.gov/...athy-aneurysms-and-muscle-cramps-syndrome - Genetics
  5. Hereditary myopathy with early respiratory failure 
    ... failure (HMERF) is an inherited disease that affects muscles used for movement (skeletal muscles) and muscles that are needed for breathing (respiratory ...
    https://medlineplus.gov/...y-myopathy-with-early-respiratory-failure - Genetics
  6. Glycogen storage disease type IX 
    ... can affect glycogen breakdown in liver cells or muscle cells or sometimes both. A lack of glycogen ... sitting, standing, or walking, and some have mild muscle weakness. Puberty is delayed in some adolescents with ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-ix - Genetics
  7. Glycogen storage disease type V 
    ... break down a complex sugar called glycogen in muscle cells. A lack of glycogen breakdown interferes with the function of muscle cells.People with GSDV typically experience fatigue, muscle ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-v - Genetics
  8. Centronuclear myopathy 
    Centronuclear myopathy is a condition characterized by muscle weakness (myopathy) and wasting (atrophy) in the skeletal muscles, which are the muscles used for movement. The severity of centronuclear myopathy varies among ...
    https://medlineplus.gov/genetics/condition/centronuclear-myopathy - Genetics
  9. Adenosine monophosphate deaminase deficiency 
    ... deficiency is a condition that can affect the muscles used for movement (skeletal muscles). In many affected individuals, AMP deaminase deficiency does ...
    https://medlineplus.gov/...nosine-monophosphate-deaminase-deficiency - Genetics
  10. Emery-Dreifuss muscular dystrophy 
    ... muscular dystrophy is a condition that primarily affects muscles used for movement (skeletal muscles) and the heart (cardiac muscle). Among the earliest ...
    https://medlineplus.gov/.../emery-dreifuss-muscular-dystrophy - Genetics
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