KEGG   DISEASE: バッテン病
エントリ  
H02275                                                             
名称    
バッテン病;
Spielmeyer-Vogt 病;
若年型神経セロイドリポフスチン症
  上位グループ
神経セロイドリポフスチン症 [DS:H00149]
進行性ミオクローヌスてんかん [DS:H00810]
ライソゾーム病 (リソソーム蓄積症) [DS:H01425]
概要    
Batten disease, also known as Juvenile neuronal ceroid lipofuscinoses (JNCL), is an autosomal recessive lysosomal disease. It manifests with vision loss, followed by seizures and progressive neurodegeneration, robbing children of motor skills, speech and cognition, and eventually leading to death in the second or third decade of life. Loss-of-function mutations in CLN3 are responsible for Batten disease.
カテゴリ  
先天性代謝異常症, ライソゾーム病
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 05 内分泌, 栄養, 代謝の疾患
  代謝疾患
   先天性代謝異常
    5C56  ライソゾーム病
     H02275  バッテン病
パスウェイ 
hsa04142  Lysosome
病因遺伝子 
CLN3 [HSA:1201] [KO:K12389]
コメント  
Although Batten disease is usually regarded as JNCL, some physicians use the term Batten disease to describe all forms of NCL.
リンク   
ICD-11: 5C56.1
MeSH: D009472
OMIM: 204200
文献    
  著者
Cotman SL, Staropoli JF
  タイトル
The juvenile Batten disease protein, CLN3, and its role in regulating anterograde and retrograde post-Golgi trafficking.
  雑誌
Clin Lipidol 7:79-91 (2012)
DOI:10.2217/clp.11.70
文献    
  著者
Adams HR, Mink JW
  タイトル
Neurobehavioral features and natural history of juvenile neuronal ceroid lipofuscinosis (Batten disease).
  雑誌
J Child Neurol 28:1128-36 (2013)
DOI:10.1177/0883073813494813
文献    
PMID:9004140
  著者
Jarvela I, Mitchison HM, Munroe PB, O'Rawe AM, Mole SE, Syvanen AC
  タイトル
Rapid diagnostic test for the major mutation underlying Batten disease.
  雑誌
J Med Genet 33:1041-2 (1996)
DOI:10.1136/jmg.33.12.1041
LinkDB    

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