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Results 1 - 10 of 61 for body myopathy
  1. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD) is a condition that can affect the muscles, ... altered gene from one affected parent. IBMPFD Inclusion body myopathy with early-onset Paget disease of bone and/ ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  2. GNE myopathy 
    ... called it rimmed vacuole myopathy or hereditary inclusion body myopathy (HIBM). It has since become clear that these ... vacuoles Distal myopathy, Nonaka type DMRV Hereditary inclusion body myopathy type 2 HIBM2 IBM2 Inclusion body myopathy type ...
    https://medlineplus.gov/genetics/condition/gne-myopathy - Genetics
  3. Myosin storage myopathy 
    ... sufficient to cause the disorder. Autosomal dominant hyaline body myopathy Genetic Testing Registry: Myosin storage myopathy Hyaline body myopathy National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/genetics/condition/myosin-storage-myopathy - Genetics
  4. Nemaline myopathy 
    ... rod disease Rod body disease Rod myopathy Rod-body myopathy Genetic Testing Registry: Actin accumulation myopathy Genetic Testing ...
    https://medlineplus.gov/genetics/condition/nemaline-myopathy - Genetics
  5. Hereditary myopathy with early respiratory failure 
    ... Noguchi S, Nonaka I, Nishino I. Necklace cytoplasmic bodies in hereditary myopathy with early respiratory failure. J Neurol Neurosurg Psychiatry. ...
    https://medlineplus.gov/...y-myopathy-with-early-respiratory-failure - Genetics
  6. Idiopathic inflammatory myopathy 
    ... Testing Registry: Myositis disease Genetic Testing Registry: Inclusion body myositis Idiopathic inflammatory myopathy National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/.../idiopathic-inflammatory-myopathy - Genetics
  7. Actin-accumulation myopathy 
    ... PubMed Schroder JM, Durling H, Laing N. Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 ( ...
    https://medlineplus.gov/.../condition/actin-accumulation-myopathy - Genetics
  8. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes 
    ... is a condition that affects many of the body's systems, particularly the brain and nervous system (encephalo-) and muscles (myopathy). The signs and symptoms of this disorder most ...
    https://medlineplus.gov/...-lactic-acidosis-and-stroke-like-episodes - Genetics
  9. Neutral lipid storage disease with myopathy 
    ... stored abnormally in organs and tissues throughout the body. People with this condition have muscle weakness (myopathy) due to the accumulation of fats in muscle ...
    https://medlineplus.gov/...utral-lipid-storage-disease-with-myopathy - Genetics
  10. Cap myopathy 
    ... affects skeletal muscles, which are muscles that the body uses for movement. People with cap myopathy have muscle weakness (myopathy) and poor muscle tone ( ...
    https://medlineplus.gov/genetics/condition/cap-myopathy - Genetics
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