KEGG   DISEASE: Currarino 症候群
エントリ  
H00463                                                             
名称    
Currarino 症候群
概要    
Currarino syndrome is a condition characterized by the combination of sacral malformation, hindgut anomaly, and presacral mass. The HLXB9 gene is responsible for the syndrome.
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
   LD2F  多発性の構造異常を伴う症候群, 主な体系の関与を伴わないもの
    H00463  Currarino 症候群
病因遺伝子 
HLXB9 [HSA:3110] [KO:K08025]
リンク   
ICD-11: LD2F.1Y
MeSH: C536221
OMIM: 176450
文献    
PMID:6789651
  著者
Currarino G, Coln D, Votteler T
  タイトル
Triad of anorectal, sacral, and presacral anomalies.
  雑誌
AJR Am J Roentgenol 137:395-8 (1981)
DOI:10.2214/ajr.137.2.395
文献    
PMID:8740138
  著者
Kochling J, Pistor G, Marzhauser Brands S, Nasir R, Lanksch WR
  タイトル
The Currarino syndrome--hereditary transmitted syndrome of anorectal, sacral and presacral anomalies. Case report and review of the literature.
  雑誌
Eur J Pediatr Surg 6:114-9 (1996)
DOI:10.1055/s-2008-1066487
文献    
  著者
Cretolle C, Pelet A, Sanlaville D, Zerah M, Amiel J, Jaubert F, Revillon Y, Baala L, Munnich A, Nihoul-Fekete C, Lyonnet S
  タイトル
Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
  雑誌
Hum Mutat 29:903-10 (2008)
DOI:10.1002/humu.20718
文献    
  著者
Hagan DM, Ross AJ, Strachan T, Lynch SA, Ruiz-Perez V, Wang YM, Scambler P, Custard E, Reardon W, Hassan S, Nixon P, Papapetrou C, Winter RM, Edwards Y, Morrison K, Barrow M, Cordier-Alex MP, Correia P, Galvin-Parton PA, Gaskill S, Gaskin KJ, Garcia-Minaur S, Gereige R, Hayward R, Homfray T
  タイトル
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.
  雑誌
Am J Hum Genet 66:1504-15 (2000)
DOI:10.1086/302899
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