KEGG   DISEASE: ボーエン-コンラディ症候群
エントリ  
H00616                                                             
名称    
ボーエン-コンラディ症候群
概要    
Bowen-Conradi syndrome (BCS) is an autosomal-recessive disorder characterized by severely impaired prenatal and postnatal growth, profound psychomotor retardation. Most patients do not survive beyond the first year of life, as a result of complications associated with reduced mobility and failure to thrive. Recently, a missense mutation in EMG1 was reported to be the cause of BCS. EMG1 is a putative methyltransferase that is required for biogenesis of the 40S subunit of the ribosome.
カテゴリ  
リボソーム病
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 20 発達異常
  多発性の発達異常または症候群
   LD20  主な特徴として中枢神経系の異常を伴う症候群
    H00616  ボーエン-コンラディ症候群
パスウェイ 
hsa03008  Ribosome biogenesis in eukaryotes
病因遺伝子 
EMG1 [HSA:10436] [KO:K14568]
リンク   
ICD-11: LD20.2
MeSH: C537081
OMIM: 211180
文献    
  著者
Armistead J, Khatkar S, Meyer B, Mark BL, Patel N, Coghlan G, Lamont RE, Liu S, Wiechert J, Cattini PA, Koetter P, Wrogemann K, Greenberg CR, Entian KD, Zelinski T, Triggs-Raine B
  タイトル
Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome.
  雑誌
Am J Hum Genet 84:728-39 (2009)
DOI:10.1016/j.ajhg.2009.04.017
文献    
  著者
Freed EF, Bleichert F, Dutca LM, Baserga SJ
  タイトル
When ribosomes go bad: diseases of ribosome biogenesis.
  雑誌
Mol Biosyst 6:481-93 (2010)
DOI:10.1039/b919670f
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