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Results 1 - 10 of 13 for Leigh syndrome with cardiomyopathy
Did you mean light syndrome with cardiomyopathy?
  1. Cytochrome c oxidase deficiency 
    ... as Leigh syndrome. The signs and symptoms of Leigh syndrome include loss of mental function, movement problems, hypertrophic cardiomyopathy, eating difficulties, and brain abnormalities. Cytochrome c oxidase ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  2. MT-TK gene 
    ... A8344G mutation develop the signs and symptoms of Leigh syndrome. More About This Health Condition A condition characterized by a weakened heart muscle (cardiomyopathy) and hearing loss is also caused by a ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  3. What Is Mitochondrial Disease (Muscular Dystrophy Association) - PDF  
    Muscular Dystrophy Association ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... PDF
    https://www.mda.org/...tochondrial_Disease_Fact_Sheet_March_2020.pdf - External Health Links
  4. Leigh syndrome 
    ... Several other features may occur in people with Leigh syndrome. Many ... hypertrophic cardiomyopathy, which is a thickening of the heart muscle ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  5. Leigh Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    National Institute of Neurological Disorders and Stroke ... Mitochondrial disorders are caused by defects in mitochondria, which are energy factories found ...
    https://www.ninds.nih.gov/.../mitochondrial-disorders#leigh-syndrome - External Health Links
  6. Mitochondrial Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    National Institute of Neurological Disorders and Stroke ... Mitochondrial disorders are caused by defects in mitochondria, which are energy factories found ...
    https://www.ninds.nih.gov/.../disorders/mitochondrial-disorders - External Health Links
  7. Mitochondrial DNA Depletion Syndrome (Alpers' Disease) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    National Institute of Neurological Disorders and Stroke ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics
    https://www.ninds.nih.gov/...s#mitochondrial-dna-depletion-syndromes - External Health Links
  8. MT-TL1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition MedlinePlus Genetics provides ... muscle is also weakened, which is known as cardiomyopathy. This abnormality prevents the heart from pumping normally. ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  9. MT-TV gene 
    ... have been identified as a rare cause of Leigh syndrome, a progressive brain disorder that typically appears in ... tRNA-Val, mitochondrial Tests of MT-TV PubMed LEIGH SYNDROME, NUCLEAR; NULS TRANSFER RNA, MITOCHONDRIAL, VALINE; MTTV NCBI ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  10. Mitochondrial complex V deficiency 
    ... pigmentosa that causes vision loss.A condition called Leigh syndrome can also be caused by mitochondrial complex V deficiency. Leigh syndrome is characterized by progressive loss of mental and ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
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