KEGG   DISEASE: Tan-Almurshedi 症候群
エントリ  
H02752                                                             
名称    
Tan-Almurshedi 症候群
概要    
Tan-Almurshedi syndrome (TANALS) is an autosomal recessive neurodevelopmental disorder with global developmental delay, primary microcephaly, short stature, and craniofacial anomalies. It has been reported that mutations in DRG1 cause this syndrome. DRG1 is a human GTPase that associates with polysomes, playing a role in translation.
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
  LD90  関連する臨床的特徴として知的発達障害を伴う病状
   H02752  Tan-Almurshedi 症候群
病因遺伝子 
DRG1 [HSA:4733] [KO:K06944]
リンク   
ICD-11: LD90.Y
OMIM: 620641
文献    
  著者
Westrip CAE, Paul F, Al-Murshedi F, Qaitoon H, Cham B, Fletcher SC, Hendrix E, Boora U, Ng AYJ, Bonnard C, Najafi M, Alawbathani S, Lambert I, Fox G, Venkatesh B, Bertoli-Avella A, Tan ES, Al-Maawali A, Reversade B, Coleman ML
  タイトル
Inactivation of DRG1, encoding a translation factor GTPase, causes a recessive neurodevelopmental disorder.
  雑誌
Genet Med 25:100893 (2023)
DOI:10.1016/j.gim.2023.100893
文献    
  著者
Perez-Arellano I, Spinola-Amilibia M, Bravo J
  タイトル
Human Drg1 is a potassium-dependent GTPase enhanced by Lerepo4.
  雑誌
FEBS J 280:3647-57 (2013)
DOI:10.1111/febs.12356
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