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Results 1 - 10 of 63 for Leigh syndrome
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  1. Leigh syndrome is a severe neurological disorder that usually becomes apparent in the first year of life. This condition is characterized by progressive loss ...
  2. Leigh Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... National Institute of Neurological ...
  3. ... Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency Leigh syndrome due to pyruvate carboxylase deficiency PC deficiency Pyruvate ...
  4. ... brain that resemble those in another condition called Leigh syndrome. These changes, which can be seen with medical ... aciduria type IV with sensorineural deafness, encephalopathy, and Leigh-like syndrome 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh- ...
  5. 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
  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
  7. 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 ...
  8. ... 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 ...
  9. ... 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 ...
  10. ... 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 ...
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