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Results 1 - 10 of 34 for Leigh syndrome
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  1. ... found in approximately 10 percent of people with Leigh syndrome. Leigh syndrome is a progressive brain disorder that usually appears ... difficulty breathing.MT-ATP6 gene mutations associated with Leigh syndrome change one DNA building block (nucleotide) in the ...
  2. ... gene have been identified a few people with Leigh syndrome. Children with this condition may experience vomiting, seizures, ... people with this disorder. A few children with Leigh syndrome caused by MT-ND5 gene variants have had ...
  3. ... gene mutations have been identified in people with Leigh syndrome, a progressive brain disorder that usually appears in ... Approximately 10 to 15 percent of people with Leigh syndrome have a mutation in the SURF1 gene. Most ...
  4. ... identified in a small number of people with Leigh syndrome, a progressive brain disorder that typically appears in ... this disorder.The SDHA gene mutations responsible for Leigh syndrome change single amino acids in the SDHA protein ...
  5. ... identified in a small number of people with Leigh syndrome, a progressive brain disorder that typically appears in ... difficulty breathing can also occur in people with Leigh syndrome.The MT-ND6 gene variant that can cause ...
  6. ... identified in a small number of people with Leigh syndrome, a progressive brain disorder that typically appears in ... disorder.The MT-ND4 variant that can cause Leigh syndrome, written as C11777A or Arg340Ser, replaces the amino ...
  7. ... 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 ...
  8. ... 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 ...
  9. ... 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 ...
  10. ... 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; LS PYRUVATE DEHYDROGENASE E1, SUBUNIT BETA; PDHB NCBI ...
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