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Results 1 - 6 of 6 for NARP syndrome
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  1. Neuropathy, ataxia, and retinitis pigmentosa 
    ... overlapping features rather than two distinct syndromes. NARP NARP syndrome Neurogenic muscle weakness, ataxia, and retinitis pigmentosa Neuropathy, ataxia, and retinitis pigmentos Genetic Testing Registry: NARP syndrome NARP syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  2. MT-ATP6 gene 
    ... C in the mitochondrial ATP6 gene associated with NARP syndrome. Genes Brain Behav. 2013 Nov;12(8):812- ... ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA. Biochem ...
    https://medlineplus.gov/genetics/gene/mt-atp6 - Genetics
  3. Mitochondrial complex V deficiency 
    ... 3 years after the onset of symptoms. Both NARP and Leigh syndrome can also have other causes. The prevalence of ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  4. Leigh syndrome 
    ... ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA. Biochem ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  5. Retinitis pigmentosa 
    ... of several other genetic syndromes, including Bardet-Biedl syndrome; Refsum disease; and neuropathy, ataxia, and retinitis pigmentosa (NARP). Retinitis pigmentosa is one of the most common ...
    https://medlineplus.gov/genetics/condition/retinitis-pigmentosa - Genetics
  6. Mitochondrial DNA 
    ... vision loss, and the other specific features of NARP. More About This Health ... syndrome (described above), deletion of mitochondrial DNA causes Pearson ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics