KEGG   DISEASE: サラセミア
エントリ  
H00228                                                             
名称    
サラセミア
  下位グループ
αサラセミア
ヘモグロビンH症
βサラセミア
遺伝性高胎児ヘモグロビン血症 (HPFH)
X連鎖αサラセミア [DS:H01752]
概要    
Thalassemia is the most common hereditary blood disease caused by mutation of genes encoding hemoglobin alpha and beta chains. The anemia that is associated with thalassemia is caused by ineffective erythropoiesis which results from apoptosis of erythroid precursors or hemolysis due to the chain imbalances.
カテゴリ  
血液疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 03 血液・造血器の疾患
  貧血または他の赤血球系疾患
   3A50  サラセミア
    H00228  サラセミア
病因遺伝子 
(Alpha) HBA1 [HSA:3039] [KO:K13822]
(Alpha) HBA2 [HSA:3040] [KO:K13822]
(Beta) HBB [HSA:3043] [KO:K13823]
(HPFH) HBG1 [HSA:3047] [KO:K13824]
(HPFH) HBG2 [HSA:3048] [KO:K13824]
(ATRX) ATRX [HSA:546] [KO:K10779]
リンク   
ICD-11: 3A50
MeSH: D017085 D017086
OMIM: 604131 613978 603902 613985 141749 141750
文献    
  著者
Leung WC, Leung KY, Lau ET, Tang MH, Chan V
  タイトル
Alpha-thalassaemia.
  雑誌
Semin Fetal Neonatal Med 13:215-22 (2008)
DOI:10.1016/j.siny.2008.02.006
文献    
  著者
Rund D, Rachmilewitz E
  タイトル
Beta-thalassemia.
  雑誌
N Engl J Med 353:1135-46 (2005)
DOI:10.1056/NEJMra050436
文献    
  著者
Schrier SL, Angelucci E
  タイトル
New strategies in the treatment of the thalassemias.
  雑誌
Annu Rev Med 56:157-71 (2005)
DOI:10.1146/annurev.med.56.082103.104718
文献    
  著者
Cohen AR, Galanello R, Pennell DJ, Cunningham MJ, Vichinsky E
  タイトル
Thalassemia.
  雑誌
Hematology Am Soc Hematol Educ Program 14-34 (2004)
DOI:10.1182/asheducation-2004.1.14
文献    
  著者
Miccio A, Blobel GA
  タイトル
Role of the GATA-1/FOG-1/NuRD pathway in the expression of human beta-like globin genes.
  雑誌
Mol Cell Biol 30:3460-70 (2010)
DOI:10.1128/MCB.00001-10
文献    
PMID:12393486 (Hemoglobin H)
  著者
Chui DH, Fucharoen S, Chan V
  タイトル
Hemoglobin H disease: not necessarily a benign disorder.
  雑誌
Blood 101:791-800 (2003)
DOI:10.1182/blood-2002-07-1975
文献    
PMID:15008259 (HBA1)
  著者
Harteveld CL, Wijermans PW, de Ree JE, Ter Hal P, Van Delft P, Van Rooijen-Nijdam IH, Rasp E, Kok PJ, Souverijn JH, Versteegh FG, Giordano PC
  タイトル
A new Hb evanston allele [alpha14(A12)Trp --> Arg] found solely, and in the presence of common alpha-thalassemia deletions, in three independent Asian cases.
  雑誌
Hemoglobin 28:1-5 (2004)
DOI:10.1081/hem-120028881
文献    
PMID:11791872 (HBA1)
  著者
Waye JS, Eng B, Patterson M, Carcao MD, Chang L, Olivieri NF, Chui DH
  タイトル
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin gene.
  雑誌
Hemoglobin 25:391-6 (2001)
DOI:10.1081/hem-100107876
文献    
PMID:8756078 (HBA2)
  著者
Ayala S, Colomer D, Aymerich M, Pujades A, Vives-Corrons JL
  タイトル
Nondeletional alpha-thalassemia: first description of alpha Hph alpha and alpha Nco alpha mutations in a Spanish population.
  雑誌
文献    
PMID:15977037 (HBB)
  著者
Ropero P, Villegas A, Martinez M, Ataulfo Gonzalez Fernandez F, Benavente C, Mateo M
  タイトル
A deletion of 11 bp (CD 131-134) in exon 3 of the beta-globin gene produces the phenotype of inclusion body beta-thalassemia.
  雑誌
Ann Hematol 84:584-7 (2005)
DOI:10.1007/s00277-004-0992-2
文献    
PMID:1124762 (HPFH)
  著者
Bethlenfalvay NC, Motulsky AG, Ringelhann B, Lehmann H, Humbert JR, Konotey-Ahulu FI
  タイトル
Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations.
  雑誌
Am J Hum Genet 27:140-54 (1975)
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