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- W2139858943 endingPage "338" @default.
- W2139858943 startingPage "323" @default.
- W2139858943 abstract "Mitochondrial disorders have a broad clinical spectrum and are genetically heterogeneous, involving two genomes. These disorders may be develop at any age, with isolated or multiple system involvement, and any pattern of inheritance. Neurological involvement is the most frequent, and concerns muscular, peripheral and central nervous system. Among these diverse signs, some are suggestive of mitochondrial disease, such as progressive external ophthalmoplegia, exercise intolerance, psychomotor regression, stroke-like episodes, refractory epilepsy and Epilepsia Partialis Continua. Others are less specific and mitochondrial hypothesis may be evocated because of either association of different neuromuscular signs or a multisystemic involvement. This review describes the wealth of this neurological and neuromuscular symptomatology through different syndromes reported in the literature, according to preponderant signs and to modes of inheritance, as key elements to guide genetics testing." @default.
- W2139858943 created "2016-06-24" @default.
- W2139858943 creator A5003491551 @default.
- W2139858943 creator A5032947031 @default.
- W2139858943 date "2014-05-01" @default.
- W2139858943 modified "2023-09-25" @default.
- W2139858943 title "An overview of neurological and neuromuscular signs in mitochondrial diseases" @default.
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