Epilepsy in mitochondrial diseases. Clinical lecture
نویسندگان
چکیده
Mitochondrial dysfunction mainly affects organs with high metabolic demand, primarily the brain. Epilepsy is a common phenotypic sign of both syndromic and non-syndromic mitochondrial diseases. in diseases poorly treatable often an unfavorable prognostic sign. Patients epilepsy are prescribed various anti-seizure medications. Mitochondriotoxic drugs should be avoided. Descriptions MELAS-syndrome, MERRF-syndrome, Leigh-syndrome, NARP-syndrome given.
منابع مشابه
Clinical manifestation of mitochondrial diseases.
Mitochondrial disorders (MD) represent a clinically, biochemically and genetically heterogeneous group of diseases associated with dysfunction of the oxidative phosphorylation system and pyruvate dehydrogenase complex. Our aim was to illustrate the most common clinical presentation of MD on the example of selected diseases and syndromes. The minimal prevalence of MD is estimated as 1 to 5,000. ...
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متن کاملEpilepsy in mitochondrial disorders
OBJECTIVES Information about epilepsy in mitochondrial disorders is scarce although a number or syndromic and non-syndromic mitochondrial disorders frequently manifest with focal or generalized seizures. Aim of the review was to describe epilepsy in syndromic and non-syndromic mitochondrial disorders with epilepsy as a dominant or collateral feature of the phenotype. METHODS Literature search...
متن کاملEpilepsy in Mitochondrial Disorders
Mitochondrial encephalopathies (MEs) are characterized by an extreme clinical heterogeneity since they can involve different systems and manifest at distinct ages with variable course. Many affected individuals display a cluster of clinical features that fall into discrete syndromes among syndromic pictures, epilepsy is relevant in myoclonic epilepsy with ragged-red fibers (MERRF), mitochondria...
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ژورنال
عنوان ژورنال: Russkij žurnal detskoj nevrologii
سال: 2023
ISSN: ['2073-8803', '2412-9178']
DOI: https://doi.org/10.17650/2073-8803-2022-17-4-63-70