KEGG   DISEASE: 動脈蛇行症候群
エントリ  
H00919                                                             
名称    
動脈蛇行症候群
概要    
Arterial tortuosity syndrome is an autosomal recessive disorder characterized by tortuosity, elongation, stenosis and aneurysm formation in the large and medium-sized arteries with defective elastic fibers of the arterial wall. Other features of this disease are characteristic face and several connective tissue manifestations. It has been speculated that arterial tortuosity syndrome is caused by the upregulation of TGF-beta signaling that stimulates vessel wall cell proliferation, but other mechanism involving disturbed transport of ascorbate, a cofactor for collagen and elastin hydroxylases, has been proposed recently.
カテゴリ  
先天奇形
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
   LD28  主な特徴として結合組織の異常を伴う症候群
    H00919  動脈蛇行症候群
病因遺伝子 
SLC2A10 [HSA:81031] [KO:K08147]
リンク   
ICD-11: LD28.Y
MeSH: C565942
OMIM: 208050
文献    
  著者
Coucke PJ, Willaert A, Wessels MW, Callewaert B, Zoppi N, De Backer J, Fox JE, Mancini GM, Kambouris M, Gardella R, Facchetti F, Willems PJ, Forsyth R, Dietz HC, Barlati S, Colombi M, Loeys B, De Paepe A
  タイトル
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome.
  雑誌
Nat Genet 38:452-7 (2006)
DOI:10.1038/ng1764
文献    
  著者
Drera B, Guala A, Zoppi N, Gardella R, Franceschini P, Barlati S, Colombi M
  タイトル
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity syndrome.
  雑誌
Am J Med Genet A 143:216-8 (2007)
DOI:10.1002/ajmg.a.31514
文献    
  著者
Segade F
  タイトル
Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection.
  雑誌
FEBS Lett 584:2990-4 (2010)
DOI:10.1016/j.febslet.2010.06.011
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