psoriasis, bulbar involvement, and diarrhoea in late merrf-syndrome due to the m.8344a>g trna(lys) mutation

نویسندگان

josef finsterer krankenanstalt rudolfstiftung, vienna, austria

gabor g kovacs institute of neurology, medical university of vienna, vienna, austria

چکیده

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منابع مشابه

Myoclonic epilepsy and ragged red fibers (MERRF) syndrome: selective vulnerability of CNS neurons does not correlate with the level of mitochondrial tRNAlys mutation in individual neuronal isolates.

Selective vulnerability of subpopulations of neurons is a striking feature of neurodegeneration. Mitochondrially transmitted diseases are no exception. In this study CNS tissues from a patient with myoclonus epilepsy and ragged red fibers (MERRF) syndrome, which results from an A to G transition of nucleotide (nt) 8344 in the mitochondrial tRNALys gene, were examined for the proportion of mutan...

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Mutation Causes Merrf Syndrome Phe a Novel Mitochondrial Trna

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Merrf Syndrome and Refractory Status Epilepticus

MERRF syndrome (or Myoclonic Epilepsy with Ragged Red Fibers) is a mitochondrial disease maternally-inherited. In this progressive disorder, status epilepticus is common and highly resistant to treatment including generalized anesthesia. We report two cases with Merrf syndrome (sister and brother), presented with status epilepticus refractory even to Thiopental, Propofol and Midazolam. In the s...

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عنوان ژورنال:
iranian journal of neurology

جلد ۱۶، شماره ۱، صفحات ۰-۰

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