KEGG   DISEASE: 赤色ぼろ線維・ミオクローヌスてんかん症候群
エントリ  
H01356                                                             
名称    
赤色ぼろ線維・ミオクローヌスてんかん症候群;
MERRF 症候群;
福原病
  上位グループ
進行性ミオクローヌスてんかん [DS:H00810]
ミトコンドリア病 [DS:H01427]
概要    
Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF) is a mitochondrial encephalomyopathy characterized by myoclonic seizures, cerebellar ataxia, myopathy, and ragged-red fibers (RRFs) on muscle biopsy. RRFs are muscle fibers with subsarcolemmal mitochondria that stained red with Gomori trichrome stain. The MERRF syndrome is most commonly caused by the A8344G mutation in the mitochondrial tRNA Lys gene.
カテゴリ  
先天性代謝異常症, ミトコンドリア病
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 08 神経系の疾患
  神経筋接合部または筋の疾患
   原発性筋疾患
    8C73  ミトコンドリアミオパチー
     H01356  赤色ぼろ線維・ミオクローヌスてんかん症候群
パスウェイ 
hsa00970  Aminoacyl-tRNA biosynthesis
hsa00190  Oxidative phosphorylation
病因遺伝子 
TRNK [HSA:4566] [KO:K14229]
TRNL1 [HSA:4567] [KO:K14228]
TRNH [HSA:4564] [KO:K14226]
TRNS1 [HSA:4574] [KO:K14233]
TRNS2 [HSA:4575] [KO:K14233]
TRNI [HSA:4565] [KO:K14227]
TRNF [HSA:4558] [KO:K14231]
TRNP [HSA:4571] [KO:K14232]
MTND5 [HSA:4540] [KO:K03883]
リンク   
ICD-11: 8C73.Y
MeSH: D017243
OMIM: 545000
文献    
PMID:1910259
  著者
Noer AS, Sudoyo H, Lertrit P, Thyagarajan D, Utthanaphol P, Kapsa R, Byrne E, Marzuki S
  タイトル
A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.
  雑誌
Am J Hum Genet 49:715-22 (1991)
文献    
  著者
Liu K, Zhao H, Ji K, Yan C
  タイトル
MERRF/MELAS overlap syndrome due to the m.3291T>C mutation.
  雑誌
Metab Brain Dis 29:139-44 (2014)
DOI:10.1007/s11011-013-9464-5
LinkDB    

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