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 1 - 10 of 14 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  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... Muscular Dystrophy Association ... 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)  
    Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... National Institute of Neurological ...
    https://www.ninds.nih.gov/.../mitochondrial-disorders#leigh-syndrome - External Health Links
  6. Mitochondrial DNA Depletion Syndrome (Alpers' Disease) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics
    https://www.ninds.nih.gov/...s#mitochondrial-dna-depletion-syndromes - External Health Links
  7. Mitochondrial Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... Muscle Disorders/Specifics ... Muscle Disorders ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders
    https://www.ninds.nih.gov/.../disorders/mitochondrial-disorders - External Health Links
  8. Kearns-Sayre Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Eye Diseases/Specifics ... Eye Diseases ... National Institute of Neurological Disorders and Stroke ... From ...
    https://www.ninds.nih.gov/...ondrial-disorders#kearns-sayre-syndrome - External Health Links
  9. 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
  10. 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; LS TRANSFER RNA, MITOCHONDRIAL, VALINE; MTTV NCBI Gene ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
previous · 1 · 2 · next