MERRF syndrome

MERRF syndrome (or myoclonic epilepsy with ragged red fibers) is a mitochondrial disease. It is extremely rare, and has varying degrees of expressivity owing to ...

的確，測定細胞中活性氧分子的含量後，我們發現MERRF患者細胞內的超氧化物陰離子之平均含量為正常人細胞的2倍左右，但是過氧化氫之平均含量是正常人的50%左右。

這個疾病，根據美國國家衛生研究院（NIH）的網頁資料，MERRF目前依照缺損的粒線體基因種類，分成四種：第一種，也是最常見的，就是MT-TK基因缺損。

MERRF (myoclonus epilepsy with ragged-red fibers) syndrome is an extremely rare disorder that appears in childhood, adolescence or adulthood ...

MERRF is a progressive multi-system syndrome usually beginning in childhood, but onset may occur in adulthood. The rate of progression varies widely. Onset and ...

Myoclonic epilepsy with ragged red fibers (MERRF) is a multisystem mitochondrial syndrome characterized by progressive myoclonus and seizures.

A rare mitochondrial oxidative phosphorylation disorder characterized by myoclonic seizures, ataxia, generalized epilepsy, muscle weakness and ragged red fibers ...

MERRF syndrome is a maternally inherited, multisystem disorder clinically characterized by myoclonus, generalized epilepsy, myopathy, cerebellar ataxia, ...

肌抽躍癲癇合併紅色襤褸肌纖維症，簡稱MERRF症候群(Myoclonic Epilepsy with Ragged Red Fibers Syndrome)，是一種罕見粒線體遺傳疾病，在患病機率約是10萬人中有1.5人， ...