SANDO: two novel mutations in POLG1 gene |
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Authors: | Gago Miguel Fernandes Rosas M J Guimarães Joana Ferreira Mariana Vilarinho Laura Castro Lígia Carpenter Stirling |
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Institution: | Hospital de Sao Joao, Neurologia, Department of Neurology, Porto, Portugal. miguelfgago@yahoo.com |
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Abstract: | Sensory ataxia with neuropathy, dysarthria and ophthalmoparesis represent the clinical triad of SANDO, a specific mitochondrial phenotype first reported in 1997 in association with multiple mitochondrial DNA deletions and mutations in POLG1 or more rarely in the C10orf2 (twinkle-helicase) gene. We report a 44-year-old man with SANDO who harboured two novel mutations (P648R/R807C) in the POLG1 gene. |
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