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Results 1 - 10 of 36 for Abnormal mitochondria in muscle tissue
  1. Kearns-Sayre syndrome 
    ... a microscope, these cells usually appear abnormal. The abnormal muscle cells contain an excess of structures called mitochondria and are known as ragged-red fibers.A ...
    https://medlineplus.gov/genetics/condition/kearns-sayre-syndrome - Genetics
  2. Progressive external ophthalmoplegia 
    ... a microscope, these cells usually appear abnormal. These abnormal muscle cells contain an excess of cell structures called mitochondria and are known as ragged-red fibers.Although ...
    https://medlineplus.gov/.../progressive-external-ophthalmoplegia - Genetics
  3. Multiminicore disease 
    ... skeletal muscle cells of many affected individuals. These abnormal regions can only been seen when muscle tissue is viewed under a microscope. Minicores are often present in cells with few or no mitochondria, which are the energy-producing centers within cells. ...
    https://medlineplus.gov/genetics/condition/multiminicore-disease - Genetics
  4. Central core disease 
    ... of the cell, in many affected individuals. These abnormal regions can only been seen when muscle tissue is viewed under a microscope. These central cores are often present in cells with few or no mitochondria, which produce energy within cells. Although the presence ...
    https://medlineplus.gov/genetics/condition/central-core-disease - Genetics
  5. Primary carnitine deficiency 
    ... within cells. Without carnitine, fatty acids cannot enter mitochondria and ... and muscles. This abnormal buildup causes the other signs and symptoms of ...
    https://medlineplus.gov/.../condition/primary-carnitine-deficiency - Genetics
  6. Carnitine-acylcarnitine translocase deficiency 
    ... long-chain fatty acids cannot be transported into mitochondria. As a ... and muscles. This abnormal buildup causes the other signs and symptoms of ...
    https://medlineplus.gov/...tine-acylcarnitine-translocase-deficiency - Genetics
  7. Barth syndrome 
    ... type 2 BTHS Cardioskeletal myopathy with neutropenia and abnormal mitochondria DNAJC19 defect MGA type 2 MGA type II ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  8. Myoclonic epilepsy with ragged-red fibers 
    ... a microscope, these cells usually appear abnormal. These abnormal muscle cells are called ragged-red fibers. Other features ... Mutations that cause MERRF impair the ability of mitochondria to make ... brain and muscles. Researchers have not determined how changes in mtDNA ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  9. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... not develop until adulthood. People with LBSL have abnormal muscle stiffness (spasticity) and difficulty with coordinating movements (ataxia). ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  10. Combined oxidative phosphorylation deficiency 1 
    ... to thrive). In some cases, affected individuals have abnormal muscle tone (increased or decreased), developmental delay, seizures, loss ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
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