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Results 1 - 10 of 63 for Leigh syndrome
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  1. Leigh syndrome 
    Leigh syndrome is a severe neurological disorder that usually becomes apparent in the first year of life. This condition is characterized by progressive loss ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  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 ...
    https://www.ninds.nih.gov/.../mitochondrial-disorders#leigh-syndrome - External Health Links
  3. Pyruvate carboxylase deficiency 
    ... Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency Leigh syndrome due to pyruvate carboxylase deficiency PC deficiency Pyruvate ...
    https://medlineplus.gov/.../pyruvate-carboxylase-deficiency - Genetics
  4. MEGDEL syndrome 
    ... 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- ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  5. Mitochondrial Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Muscle Disorders/Specifics ... Muscle Disorders ... Mitochondrial Diseases/Start Here ... Mitochondrial Diseases
    https://www.ninds.nih.gov/.../disorders/mitochondrial-disorders - External Health Links
  6. Mitochondrial DNA Depletion Syndrome (Alpers' Disease) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... Degenerative Nerve Diseases/Specifics ... Degenerative ...
    https://www.ninds.nih.gov/...s#mitochondrial-dna-depletion-syndromes - External Health Links
  7. Kearns-Sayre Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Eye Diseases/Specifics ... Eye Diseases ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... National Institute of Neurological Disorders and Stroke ... From ...
    https://www.ninds.nih.gov/...ondrial-disorders#kearns-sayre-syndrome - External Health Links
  8. MT-ATP6 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/mt-atp6 - Genetics
  9. MT-ND5 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/mt-nd5 - Genetics
  10. SURF1 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/surf1 - Genetics
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