KEGG   DISEASE: LADD 症候群
エントリ  
H00642                                                             
名称    
LADD 症候群;
レビーホリスター症候群
概要    
Lacrimo-auriculo-dento-digital (LADD) syndrome is an autosomal dominant disorder characterized by hypoplasia or aplasia of the lacrimal and salivary glands, cup shaped pinnae with sensorineural deafness, dental abnormalities with small teeth, and radial ray abnormalities in hands.
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
   LD27  主な特徴として皮膚または粘膜の異常を伴う症候群
    H00642  LADD 症候群
パスウェイ 
hsa04020  Calcium signaling pathway
hsa04151  PI3K-Akt signaling pathway
hsa04010  MAPK signaling pathway
hsa04810  Regulation of actin cytoskeleton
hsa04015  Rap1 signaling pathway
hsa04144  Endocytosis
hsa04550  Signaling pathways regulating pluripotency of stem cells
病因遺伝子 
(LADD1) FGFR2 [HSA:2263] [KO:K05093]
(LADD2) FGFR3 [HSA:2261] [KO:K05094]
(LADD3) FGF10 [HSA:2255] [KO:K04358]
リンク   
ICD-11: LD27.0Y
MeSH: C538132
OMIM: 149730 620192 620193
文献    
PMID:8411061
  著者
Lacombe D, Serville F, Marchand D, Battin J
  タイトル
Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromes.
  雑誌
J Med Genet 30:700-3 (1993)
DOI:10.1136/jmg.30.8.700
文献    
PMID:17682060 (FGF10, FGFR2)
  著者
Shams I, Rohmann E, Eswarakumar VP, Lew ED, Yuzawa S, Wollnik B, Schlessinger J, Lax I
  タイトル
Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast growth factor 10 (FGF10)-FGF receptor 2 signaling pathway.
  雑誌
Mol Cell Biol 27:6903-12 (2007)
DOI:10.1128/MCB.00544-07
文献    
PMID:16501574 (FGF10, FGFR2, FGFR3)
  著者
Rohmann E, Brunner HG, Kayserili H, Uyguner O, Nurnberg G, Lew ED, Dobbie A, Eswarakumar VP, Uzumcu A, Ulubil-Emeroglu M, Leroy JG, Li Y, Becker C, Lehnerdt K, Cremers CW, Yuksel-Apak M, Nurnberg P, Kubisch C, Schlessinger J, van Bokhoven H, Wollnik B
  タイトル
Mutations in different components of FGF signaling in LADD syndrome.
  雑誌
Nat Genet 38:414-7 (2006)
DOI:10.1038/ng1757
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