KEGG   DISEASE: 低身長、成長遅滞、先天性心疾患
エントリ  
H02439                                                             
名称    
低身長、成長遅滞、先天性心疾患
概要    
Short stature, developmental delay, congenital heart defect (SDDHD) is an autosomal recessive syndrome caused by mutations in TKT, that encodes transketolase. Transketolase is a thiamine-dependent enzyme in the pentose phosphate pathway. Transketolase deficiency reduces NADPH synthesis and nucleic acid synthesis and cell division and could explain the problems with growth.
カテゴリ  
先天性代謝異常症
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 05 内分泌, 栄養, 代謝の疾患
  代謝疾患
   先天性代謝異常
    5C51  糖質代謝の先天性異常
     H02439  低身長、成長遅滞、先天性心疾患
パスウェイ 
hsa00030  Pentose phosphate pathway
病因遺伝子 
TKT [HSA:7086] [KO:K00615]
リンク   
ICD-11: 5C51.0
OMIM: 617044
文献    
  著者
Boyle L, Wamelink MMC, Salomons GS, Roos B, Pop A, Dauber A, Hwa V, Andrew M, Douglas J, Feingold M, Kramer N, Saitta S, Retterer K, Cho MT, Begtrup A, Monaghan KG, Wynn J, Chung WK
  タイトル
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects.
  雑誌
Am J Hum Genet 98:1235-1242 (2016)
DOI:10.1016/j.ajhg.2016.03.030
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