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KEGG   DISEASE: Multiple synostosis syndrome
Entry
H00484                      Disease                                
Name
Multiple synostosis syndrome
Description
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.
Category
Congenital malformation
Brite
Human diseases in ICD-11 classification [BR:br08403]
 20 Developmental anomalies
  Structural developmental anomalies primarily affecting one body system
   Structural developmental anomalies of the skeleton
    LB90  Joint formation defects
     H00484  Multiple synostosis syndrome
Pathway-based classification of diseases [BR:br08402]
 Signal transduction
  nt06507  TGFB signaling
   H00484  Multiple synostosis syndrome
Pathway
hsa04350  TGF-beta signaling pathway
Network
nt06507 TGFB signaling
Gene
(SYNS1) NOG [HSA:9241] [KO:K04658]
(SYNS2) GDF5 [HSA:8200] [KO:K04664]
(SYNS3) FGF9 [HSA:2254] [KO:K04358]
(SYNS4) GDF6 [HSA:392255] [KO:K20012]
Other DBs
ICD-11: LB90.Y
ICD-10: Q78.8
MeSH: C536943 C537380 C567839
OMIM: 186500 610017 612961 617898
Reference
PMID:7428777
  Authors
Pedersen JC, Fryns JP, Carpentier G, Heremans G, Van den Berghe H
  Title
Multiple synostosis syndrome.
  Journal
Eur J Pediatr 134:273-5 (1980)
DOI:10.1007/BF00441486
Reference
PMID:10080184 (SYNS1)
  Authors
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
  Title
Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.
  Journal
Nat Genet 21:302-4 (1999)
DOI:10.1038/6821
Reference
PMID:16532400 (SYNS2)
  Authors
Dawson K, Seeman P, Sebald E, King L, Edwards M, Williams J 3rd, Mundlos S, Krakow D
  Title
GDF5 is a second locus for multiple-synostosis syndrome.
  Journal
Am J Hum Genet 78:708-12 (2006)
DOI:10.1086/503204
Reference
PMID:19589401 (SYNS3)
  Authors
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
  Title
Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.
  Journal
Am J Hum Genet 85:53-63 (2009)
DOI:10.1016/j.ajhg.2009.06.007
Reference
PMID:26643732 (SYNS4)
  Authors
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
  Title
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.
  Journal
J Bone Miner Res 31:882-9 (2016)
DOI:10.1002/jbmr.2761
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