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Results 1 - 10 of 18 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. 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
  3. 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
  4. 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
  5. 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
  6. 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
  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. Dihydrolipoamide dehydrogenase deficiency 
    ... Leber SM, Martin DM, Thoene JG, Bedoyan JK. Leigh syndrome in a girl with a novel DLD mutation ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics
  9. Primary ciliary dyskinesia 
    ... 649038. Epub 2007 May 21. Citation on PubMed Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genet Med. 2009 Jul;11(7):473-87. ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
  10. Kindler epidermolysis bullosa 
    ... R, Al-Ismaily A, Atherton DJ, Harwood CA, Leigh IM, Moss C, Didona B, Zambruno G, ... disorder, Kindler syndrome. J Invest Dermatol. 2004 Jan;122(1):78- ...
    https://medlineplus.gov/.../condition/kindler-epidermolysis-bullosa - Genetics
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