KEGG   DISEASE: 早期発症進行性脳症
エントリ  
H02472                                                             
名称    
早期発症進行性脳症
  下位グループ
脳萎縮と拘縮を伴う早期発症進行性脳症 (PEBAS)
突発性横紋筋融解症を伴う早期発症進行性脳症 (PEERB)
概要    
Early-onset progressive encephalopathy with brain atrophy and spasticity (PEBAS) is caused by mutations in TRAPPC12. Changes in Golgi morphology, membrane trafficking dysfunction, and mitotic delay were reported in fibroblasts of patients.Early-onset progressive encephalopathy with episodic rhabdomyolysis (PEERB) is caused by mutations in TRAPPC2L. Both TRAPPC2L and TRAPPC12 are members of the TRAPP protein complex, which functions in membrane trafficking.
カテゴリ  
神経系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 08 神経系の疾患
  てんかんまたは発作
   8A62  てんかん性脳症
    H02472  早期発症進行性脳症
病因遺伝子 
(PEBAS) TRAPPC12 [HSA:51112] [KO:K20309]
(PEERB) TRAPPC2L [HSA:51693] [KO:K20301]
リンク   
ICD-11: 8A62.Y
OMIM: 617669 618331
文献    
  著者
Milev MP, Grout ME, Saint-Dic D, Cheng YH, Glass IA, Hale CJ, Hanna DS, Dorschner MO, Prematilake K, Shaag A, Elpeleg O, Sacher M, Doherty D, Edvardson S
  タイトル
Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction.
  雑誌
Am J Hum Genet 101:291-299 (2017)
DOI:10.1016/j.ajhg.2017.07.006
文献    
  著者
Milev MP, Graziano C, Karall D, Kuper WFE, Al-Deri N, Cordelli DM, Haack TB, Danhauser K, Iuso A, Palombo F, Pippucci T, Prokisch H, Saint-Dic D, Seri M, Stanga D, Cenacchi G, van Gassen KLI, Zschocke J, Fauth C, Mayr JA, Sacher M, van Hasselt PM
  タイトル
Bi-allelic mutations in TRAPPC2L result in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts.
  雑誌
J Med Genet 55:753-764 (2018)
DOI:10.1136/jmedgenet-2018-105441
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