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Results 1 - 10 of 41 for Leigh "syndrome," mitochondrial
Did you mean light "syndrome," mitochondrial?
  1. Leigh syndrome 
    ... Genetic Testing Registry: Leigh Syndrome (nuclear DNA mutation) Leigh syndrome Mitochondrial DNA-associated Leigh syndrome National Organization for Rare ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  2. MT-ND5 gene 
    ... Sudo A, Honzawa S, Nonaka I, Goto YI. Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in ...
    https://medlineplus.gov/genetics/gene/mt-nd5 - Genetics
  3. 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
  4. 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 ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  5. MT-TV gene 
    ... tRNA-Val, mitochondrial Tests of MT-TV PubMed LEIGH SYNDROME, NUCLEAR; NULS TRANSFER RNA, MITOCHONDRIAL, VALINE; MTTV NCBI Gene ClinVar Blakely EL, Poulton ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  6. Mitochondrial DNA 
    ... oxidative phosphorylation. For example, the most commonly mutated mitochondrial gene in Leigh syndrome, MT-ATP6, provides instructions for a protein that ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  7. Mitochondrial complex I deficiency 
    ... a specific syndrome. For example, a condition called Leigh syndrome is most commonly caused by mitochondrial complex I deficiency. Leigh syndrome is characterized by ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  8. MT-ATP6 gene 
    ... Gene ClinVar Ball M, Thorburn DR, Rahman S. Mitochondrial DNA-Associated Leigh Syndrome Spectrum. 2003 Oct 30 [updated 2024 May 9]. ... may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the ... A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal ...
    https://medlineplus.gov/genetics/gene/mt-atp6 - Genetics
  9. Find a Neuromuscular Disease (Muscular Dystrophy Association)  
    Neuromuscular Disorders/Start Here ... Neuromuscular Disorders ... Muscular Dystrophy Association ... MDA is the #1 health nonprofit advancing research, care and advocacy ...
    https://www.mda.org/disease/list - External Health Links
  10. Neuropathy, ataxia, and retinitis pigmentosa 
    ... PIGMENTOSA PubMed Ball M, Thorburn DR, Rahman S. Mitochondrial DNA-Associated Leigh Syndrome Spectrum. 2003 Oct 30 [updated 2024 May 9]. ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
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