KEGG   DISEASE: 多発性骨癒合症症候群
エントリ  
H00484                                                             
名称    
多発性骨癒合症症候群
概要    
Proximal symphalangism is a condition characterized by variable fusion of the proximal interphalangeal joints. Multiple synostosis syndrome (SYNS) is a more severe form of proximal symphalangism with additional bone fusions involving carpal, tarsal, and other joints.
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
  主に1つの体系に影響する構造的発達異常
   骨格の構造的発達異常
    LB90  関節形成障害
     H00484  多発性骨癒合症症候群
パスウェイに基づく疾患分類 [BR:jp08402]
 シグナル伝達
  nt06507  TGFB シグナリング
   H00484  多発性骨癒合症症候群
パスウェイ 
hsa04350  TGF-beta signaling pathway
ネットワーク
nt06507 TGFB signaling
病因遺伝子 
(SYNS1) NOG [HSA:9241] [KO:K04658]
(SYNS2) GDF5 [HSA:8200] [KO:K04664]
(SYNS3) FGF9 [HSA:2254] [KO:K04358]
(SYNS4) GDF6 [HSA:392255] [KO:K20012]
リンク   
ICD-11: LB90.Y
MeSH: C536943 C537380 C567839
OMIM: 186500 610017 612961 617898
文献    
PMID:7428777
  著者
Pedersen JC, Fryns JP, Carpentier G, Heremans G, Van den Berghe H
  タイトル
Multiple synostosis syndrome.
  雑誌
Eur J Pediatr 134:273-5 (1980)
DOI:10.1007/BF00441486
文献    
PMID:10080184 (SYNS1)
  著者
Gong Y, Krakow D, Marcelino J, Wilkin D, Chitayat D, Babul-Hirji R, Hudgins L, Cremers CW, Cremers FP, Brunner HG, Reinker K, Rimoin DL, Cohn DH, Goodman FR, Reardon W, Patton M, Francomano CA, Warman ML
  タイトル
Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.
  雑誌
Nat Genet 21:302-4 (1999)
DOI:10.1038/6821
文献    
PMID:16532400 (SYNS2)
  著者
Dawson K, Seeman P, Sebald E, King L, Edwards M, Williams J 3rd, Mundlos S, Krakow D
  タイトル
GDF5 is a second locus for multiple-synostosis syndrome.
  雑誌
Am J Hum Genet 78:708-12 (2006)
DOI:10.1086/503204
文献    
PMID:19589401 (SYNS3)
  著者
Wu XL, Gu MM, Huang L, Liu XS, Zhang HX, Ding XY, Xu JQ, Cui B, Wang L, Lu SY, Chen XY, Zhang HG, Huang W, Yuan WT, Yang JM, Gu Q, Fei J, Chen Z, Yuan ZM, Wang ZG
  タイトル
Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.
  雑誌
Am J Hum Genet 85:53-63 (2009)
DOI:10.1016/j.ajhg.2009.06.007
文献    
PMID:26643732 (SYNS4)
  著者
Wang J, Yu T, Wang Z, Ohte S, Yao RE, Zheng Z, Geng J, Cai H, Ge Y, Li Y, Xu Y, Zhang Q, Gusella JF, Fu Q, Pregizer S, Rosen V, Shen Y
  タイトル
A New Subtype of Multiple Synostoses Syndrome Is Caused by a Mutation in GDF6 That Decreases Its Sensitivity to Noggin and Enhances Its Potency as a BMP Signal.
  雑誌
J Bone Miner Res 31:882-9 (2016)
DOI:10.1002/jbmr.2761
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