KEGG   DISEASE: 胎児または新生児のRh溶血性疾患
エントリ  
H02799                                                             
名称    
胎児または新生児のRh溶血性疾患
概要    
Rh-induced hemolytic disease of the fetus and newborn (HDFNRH) is one of IgG- mediated red cell destruction. When an RhD negative mother is exposed to the RhD positive red cells, she develops allo-anti-D which crosses the placenta and then results in the destruction of fetal red cells. Clinical manifestations of HDFNRH range from asymptomatic mild anaemia to hydrops fetalis or stillbirth associated with severe anaemia and jaundice. The antigens of the Rh blood group are carried by proteins coded by 2 genes, RHD and RHCE. In whites, the vast majority of D-negative haplotypes are due to a deletion of the RHD gene.
カテゴリ  
血液疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 19 周産期に発生した病態
  胎児または新生児の出血性疾患または血液疾患
   KA84  胎児または新生児の溶血性疾患
    H02799  胎児または新生児のRh溶血性疾患
病因遺伝子 
RHD [HSA:6007] [KO:K06579]
リンク   
ICD-11: KA84.0
OMIM: 619462
文献    
  著者
Urbaniak SJ, Greiss MA
  タイトル
RhD haemolytic disease of the fetus and the newborn.
  雑誌
Blood Rev 14:44-61 (2000)
DOI:10.1054/blre.1999.0123
文献    
  著者
Christensen RD, Bahr TM, Ilstrup SJ, Dizon-Townson DS
  タイトル
Alloimmune hemolytic disease of the fetus and newborn: genetics, structure, and function of the commonly involved erythrocyte antigens.
  雑誌
J Perinatol 43:1459-1467 (2023)
DOI:10.1038/s41372-023-01785-3
文献    
  著者
Wagner FF, Flegel WA
  タイトル
RHD gene deletion occurred in the Rhesus box.
  雑誌
Blood 95:3662-8 (2000)
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