نتایج جستجو برای: mitochondrial encephalomyopathy

تعداد نتایج: 132426  

Journal: :American journal of human genetics 2008
Daniele Ghezzi Ann Saada Pio D'Adamo Erika Fernandez-Vizarra Paolo Gasparini Valeria Tiranti Orly Elpeleg Massimo Zeviani

In two siblings we found a mitochondrial encephalomyopathy, characterized by developmental delay, hemiplegia, convulsions, asymmetrical brain atrophy, and low cytochrome c oxidase (COX) activity in skeletal muscle. The disease locus was identified on chromosome 2 by homozygosity mapping; candidate genes were prioritized for their known or predicted mitochondrial localization and then sequenced ...

Journal: :Current opinion in genetics & development 2016
Matthew J Young William C Copeland

The human mitochondrial genome is replicated by DNA polymerase γ in concert with key components of the mitochondrial DNA (mtDNA) replication machinery. Defects in mtDNA replication or nucleotide metabolism cause deletions, point mutations, or depletion of mtDNA. The resulting loss of cellular respiration ultimately induces mitochondrial genetic diseases, including mtDNA depletion syndromes (MDS...

Journal: :Arquivos de neuro-psiquiatria 1989
A Cukiert F G Naylor H B Scapolan M M Vilela F S Aloe J O Siffert A M Tsanaclis M Haddad T C Machado M Carvalho-Alegro

Two brothers presented to us with a progressive myoclonic syndrome with slight cerebellar symptoms. Neurological examination disclosed moderate cerebellar signs and pale optic discs; asymmetric, asynchronous and arrhythmic myoclonus, an arrthesthesic deficit and no muscular weakness. EEG background activity was moderately slow with no irritative discharges. CT was normal in both cases. Intermit...

Journal: :Brain : a journal of neurology 2008
Alexandra Götz Pirjo Isohanni Helena Pihko Anders Paetau Riitta Herva Outi Saarenpää-Heikkilä Leena Valanne Sanna Marjavaara Anu Suomalainen

Mitochondrial DNA depletion syndrome (MDS) is a severe recessively inherited disease of childhood. It manifests most often in infancy, is rapidly progressive and leads to early death. MDS is caused by an increasing number of nuclear genes leading to multisystemic or tissue-specific decrease in mitochondrial DNA (mtDNA) copy number. Thymidine kinase 2 (TK2) has been reported to cause a myopathic...

2016
Sara Seitun Laura Massobrio Anna Rubegni Claudia Nesti Margherita Castiglione Morelli Sara Boccalini Athena Galletto Pregliasco Irilda Budaj Luca Deferrari Gian Marco Rosa Fabrizio Montecucco Alberto Valbusa

A 49-year-old man presented with chest pain, dyspnea, and lactic acidosis. Left ventricular hypertrophy and myocardial fibrosis were detected. The sequencing of mitochondrial genome (mtDNA) revealed the presence of A to G mtDNA point mutation at position 3243 (m.3243A>G) in tRNALeu(UUR) gene. Diagnosis of cardiac involvement in a patient with Mitochondrial Encephalomyopathy, Lactic Acidosis, an...

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