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Results 1 - 9 of 9 for Leigh syndrome due to mitochondrial complex I deficiency
Did you mean light syndrome due to mitochondrial complex I deficiency?
  1. Mitochondrial complex I deficiency 
    ... most commonly caused by mitochondrial complex I deficiency. Leigh syndrome ... vision problems due to optic nerve degeneration. These syndromes can also ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  2. Leigh syndrome 
    ... ClinicalTrials.gov NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5 LEIGH SYNDROME; LS PubMed Ball M, Thorburn DR, Rahman S. ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  3. MT-ATP6 gene 
    ... likely cause the characteristic signs and symptoms of Leigh syndrome. More About This Health Condition MedlinePlus Genetics provides information about Mitochondrial complex V deficiency More About This Health Condition Some of the ...
    https://medlineplus.gov/genetics/gene/mt-atp6 - Genetics
  4. BCS1L gene 
    ... available energy likely leads to the features of mitochondrial complex III deficiency. More About This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition BC1 (ubiquinol-cytochrome ...
    https://medlineplus.gov/genetics/gene/bcs1l - Genetics
  5. MT-ND1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition MedlinePlus Genetics provides information about Mitochondrial complex I deficiency More About This Health Condition A mutation in ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
  6. MT-TL1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition MedlinePlus Genetics provides information about Mitochondrial complex I deficiency More About This Health Condition About 20 mutations ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  7. Cytochrome c oxidase deficiency 
    ... IV deficiency COX deficiency Cytochrome-c oxidase deficiency Mitochondrial complex IV deficiency Genetic Testing Registry: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Genetic Testing ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  8. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
    https://medlineplus.gov/geneticbraindisorders.html - Health Topics
  9. GFM1 gene 
    ... Rodenburg RJ. Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1. JIMD Rep. 2012; ...
    https://medlineplus.gov/genetics/gene/gfm1 - Genetics