Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 21 - 30 of 36 for Abnormal mitochondria in muscle tissue
  1. Deafness-dystonia-optic neuronopathy syndrome 
    ... abnormal protein transport, although it is unclear how abnormal protein transport affects the function of the mitochondria and causes the signs and symptoms of DDON ...
    https://medlineplus.gov/...ness-dystonia-optic-neuronopathy-syndrome - Genetics
  2. Alpers-Huttenlocher syndrome 
    ... in nerve function (neuropathy). Neuropathy can lead to abnormal or absent reflexes (areflexia). In addition, affected individuals may develop weak muscle tone (hypotonia) that worsens until they lose the ...
    https://medlineplus.gov/.../condition/alpers-huttenlocher-syndrome - Genetics
  3. Mitochondrial complex I deficiency 
    ... I deficiency typically have neurological problems, such as abnormal brain ... low muscle tone (hypotonia), muscle pain (myalgia), and extreme fatigue ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  4. Friedreich ataxia 
    ... hypertrophic cardiomyopathy, which enlarges and weakens the heart muscle and can be life-threatening. Some affected individuals develop diabetes or an abnormal curvature of the spine (scoliosis).Most people with ...
    https://medlineplus.gov/genetics/condition/friedreich-ataxia - Genetics
  5. Spastic paraplegia type 7 
    ... movements of the eyes (nystagmus); mild hearing loss; abnormal curvature of ... muscle movement (motor neuropathy); and muscle wasting (amyotrophy). The ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  6. Mitochondrial complex V deficiency 
    ... affected individuals, and in some cases result in abnormal brain function ... of the heart (cardiac) muscle that can lead to heart failure. People with ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  7. 2-hydroxyglutaric aciduria 
    ... gene provides instructions for making an enzyme in mitochondria that normally produces a different compound. When the enzyme is altered by mutations, it takes on a new, abnormal function: production of the potentially toxic compound D- ...
    https://medlineplus.gov/.../condition/2-hydroxyglutaric-aciduria - Genetics
  8. Leukoencephalopathy with thalamus and brainstem involvement and high lactate 
    ... weak muscle tone (hypotonia), involuntary muscle tensing (dystonia), muscle spasticity, and seizures. Some have extremely high levels of lactate (lactic acidosis), which can cause serious breathing problems and an abnormal heartbeat. Liver failure occurs in some severely affected ...
    https://medlineplus.gov/...nd-brainstem-involvement-and-high-lactate - Genetics
  9. Pearson syndrome 
    ... Kearns-Sayre syndrome. This condition causes weakness of muscles around the eyes and other problems. Pearson syndrome is a rare condition; its prevalence is unknown. Pearson syndrome is caused by defects in mitochondria, which are structures within cells that use oxygen ...
    https://medlineplus.gov/genetics/condition/pearson-syndrome - Genetics
  10. Pantothenate kinase-associated neurodegeneration 
    ... typically beginning in childhood. Movement abnormalities include involuntary ... is characterized by an abnormal buildup of iron in certain areas of the ...
    https://medlineplus.gov/...enate-kinase-associated-neurodegeneration - Genetics
previous · 1 · 2 · 3 · 4 · next