KEGG   DISEASE: 無四肢症候群
エントリ  
H00636                                                             
名称    
無四肢症候群
概要    
Tetra-amelia syndrome (TETAMS) is an extremely rare condition characterized by the complete absence of all four limbs. Patients commonly have other anomalies involving the face, eyes, heart, nervous system, and urogenital system. Homozygous Wnt3 mutation is responsible for tetra-amelia. Recently, it has been reported that RSPO2 mutations cause tetra-amelia syndrome with lung aplasia.
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
    LB9B  上肢及び下肢の減形成
     H00636  無四肢症候群
パスウェイに基づく疾患分類 [BR:jp08402]
 シグナル伝達
  nt06505  WNT シグナリング
   H00636  無四肢症候群
パスウェイ 
hsa04310  Wnt signaling pathway
ネットワーク
nt06505 WNT signaling
病因遺伝子 
(TETAMS1) WNT3 [HSA:7473] [KO:K00312]
(TETAMS2) RSPO2 [HSA:340419] [KO:K23097]
リンク   
ICD-11: LB9B
ICD-10: Q73.0
MeSH: C536498
OMIM: 273395 618021
文献    
  著者
Niemann S
  タイトル
Tetra-Amelia Syndrome
  雑誌
GeneReviews (1993)
文献    
  著者
Niemann S, Zhao C, Pascu F, Stahl U, Aulepp U, Niswander L, Weber JL, Muller U
  タイトル
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family.
  雑誌
Am J Hum Genet 74:558-63 (2004)
DOI:10.1086/382196
文献    
  著者
Al-Qattan MM
  タイトル
WNT pathways and upper limb anomalies.
  雑誌
J Hand Surg Eur Vol 36:9-22 (2011)
DOI:10.1177/1753193410380502
文献    
  著者
Szenker-Ravi E, Altunoglu U, Leushacke M, Bosso-Lefevre C, Khatoo M, Thi Tran H, Naert T, Noelanders R, Hajamohideen A, Beneteau C, de Sousa SB, Karaman B, Latypova X, Basaran S, Yucel EB, Tan TT, Vlaminck L, Nayak SS, Shukla A, Girisha KM, Le Caignec C, Soshnikova N, Uyguner ZO, Vleminckx K, Barker N, Kayserili H, Reversade B
  タイトル
RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6.
  雑誌
Nature 557:564-569 (2018)
DOI:10.1038/s41586-018-0118-y
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