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Results 11 - 20 of 54 for Leigh syndrome
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  1. Cytochrome c oxidase deficiency 
    ... have a specific group of features known as Leigh syndrome. The signs and symptoms of Leigh syndrome include loss of mental function, movement problems, hypertrophic ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  2. 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
  3. Neuropathy, ataxia, and retinitis pigmentosa 
    ... common than a similar but more severe condition, Leigh syndrome, which affects about 1 in 40,000 people. ... a more severe condition known as maternally inherited Leigh syndrome. Because these two conditions result from the same ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  4. MT-TK gene 
    ... can also cause a progressive brain disorder called Leigh syndrome. Signs and symptoms of this condition usually begin ... A8344G mutation develop the signs and symptoms of Leigh syndrome. More About This Health Condition A condition characterized ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  5. SLC19A3 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition SLC19A3 gene mutations ... symptoms similar to those of the neurological disorders Leigh syndrome and Wernicke encephalopathy have also been found to ...
    https://medlineplus.gov/genetics/gene/slc19a3 - Genetics
  6. 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
  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 progressive loss of mental and ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  8. PDHB gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition ODPB_HUMAN PDHBD ... dehydrogenase, E1 beta polypeptide Tests of PDHB PubMed LEIGH SYNDROME, NUCLEAR; NULS PYRUVATE DEHYDROGENASE E1, SUBUNIT BETA; PDHB ...
    https://medlineplus.gov/genetics/gene/pdhb - Genetics
  9. SERAC1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition FLJ14917 protein SERAC1 ... aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1. Am J ...
    https://medlineplus.gov/genetics/gene/serac1 - Genetics
  10. SUCLA2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition A-BETA A- ... SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like ... Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria. 2009 May 26 [ ...
    https://medlineplus.gov/genetics/gene/sucla2 - Genetics
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