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Results 1 - 9 of 9 for Leigh syndrome with cardiomyopathy
Did you mean light syndrome with cardiomyopathy?
  1. Cytochrome c oxidase deficiency 
    ... as Leigh syndrome. The signs and symptoms of Leigh syndrome include loss of mental function, movement problems, hypertrophic cardiomyopathy, eating difficulties, and brain abnormalities. Cytochrome c oxidase ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  2. MT-TK gene 
    ... A8344G mutation develop the signs and symptoms of Leigh syndrome. More About This Health Condition A condition characterized by a weakened heart muscle (cardiomyopathy) and hearing loss is also caused by a ...
    https://medlineplus.gov/genetics/gene/mt-tk - Genetics
  3. Leigh syndrome 
    ... Several other features may occur in people with Leigh syndrome. Many ... hypertrophic cardiomyopathy, which is a thickening of the heart muscle ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  4. MT-TL1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition MedlinePlus Genetics provides ... muscle is also weakened, which is known as cardiomyopathy. This abnormality prevents the heart from pumping normally. ...
    https://medlineplus.gov/genetics/gene/mt-tl1 - Genetics
  5. 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; LS TRANSFER RNA, MITOCHONDRIAL, VALINE; MTTV NCBI Gene ...
    https://medlineplus.gov/genetics/gene/mt-tv - Genetics
  6. 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
  7. DSP gene 
    ... form of heart disease called dilated left ventricular cardiomyopathy.The DSP gene mutations that cause keratoderma with ... that abnormal cell signaling may also contribute to cardiomyopathy in people with this condition. More About This ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  8. Keratoderma with woolly hair 
    ... the feet to become thick, scaly, and calloused.Cardiomyopathy, which is a disease of the heart muscle, ... features of this condition, signs and symptoms of cardiomyopathy may not appear until adolescence or later. Complications ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  9. 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