KEGG   DISEASE: 乏毛症・リンパ浮腫・毛細血管拡張症症候群
エントリ  
H02168                                                             
名称    
乏毛症・リンパ浮腫・毛細血管拡張症症候群
概要    
Hypotrichosis-lymphedema-telangiectasia syndrome (HLTS) is an extremely rare lymphedema syndrome. The transcription factor SOX18 was shown to play a role in the development of hair, blood vessels and lymphatic vessels. SOX18 mutations are associated with both recessive and dominant HLTS.
カテゴリ  
先天奇形
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 11 循環器系の疾患
  リンパ管またはリンパ節の疾患
   BD93  リンパ浮腫
    H02168  乏毛症・リンパ浮腫・毛細血管拡張症症候群
病因遺伝子 
SOX18 [HSA:54345] [KO:K09270]
リンク   
ICD-11: BD93.0
MeSH: C564327
OMIM: 137940 607823
文献    
  著者
Downes M, Francois M, Ferguson C, Parton RG, Koopman P
  タイトル
Vascular defects in a mouse model of hypotrichosis-lymphedema-telangiectasia syndrome indicate a role for SOX18 in blood vessel maturation.
  雑誌
Hum Mol Genet 18:2839-50 (2009)
DOI:10.1093/hmg/ddp219
文献    
  著者
Wunnemann F, Kokta V, Leclerc S, Thibeault M, McCuaig C, Hatami A, Stheneur C, Grenier JC, Awadalla P, Mitchell GA, Andelfinger G, Preuss C
  タイトル
Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.
  雑誌
Can J Cardiol 32:135.e1-7 (2016)
DOI:10.1016/j.cjca.2015.04.004
文献    
  著者
Moalem S, Brouillard P, Kuypers D, Legius E, Harvey E, Taylor G, Francois M, Vikkula M, Chitayat D
  タイトル
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene.
  雑誌
Clin Genet 87:378-82 (2015)
DOI:10.1111/cge.12388
LinkDB    

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