KEGG   DISEASE: 家族性偽高カリウム血症
エントリ  
H02001                                                             
名称    
家族性偽高カリウム血症
  上位グループ
遺伝性有口赤血球症 [DS:H00232]
概要    
Familial pseudohyperkalaemia (PSHK) is an autosomal dominant red cell trait characterized by increased serum potassium in whole blood stored at or below room temperature, as a result of a temperature-based abnormality in the transport of potassium across the red cell membrane. PSHK is not accompanied by clinical symptoms or biological signs except for borderline abnormalities of red cell shape.
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
   溶血性貧血
    先天性溶血性貧血
     3A10  遺伝性溶血性貧血
      H02001  家族性偽高カリウム血症
パスウェイ 
hsa02010  ABC transporters
病因遺伝子 
(PSHK1) PIEZO1 [HSA:9780] [KO:K22128]
(PSHK2) ABCB6 [HSA:10058] [KO:K05661]
リンク   
ICD-11: 3A10.3
MeSH: C563785
OMIM: 194380 609153
文献    
  著者
Gore DM, Chetty MC, Fisher J, Nicolaou A, Stewart GW
  タイトル
Familial pseudohyperkalaemia Cardiff: a mild version of cryohydrocytosis.
  雑誌
Br J Haematol 117:212-4 (2002)
DOI:10.1046/j.1365-2141.2002.03376.x
文献    
  著者
Andolfo I, Alper SL, Delaunay J, Auriemma C, Russo R, Asci R, Esposito MR, Sharma AK, Shmukler BE, Brugnara C, De Franceschi L, Iolascon A
  タイトル
Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.
  雑誌
Am J Hematol 88:66-72 (2013)
DOI:10.1002/ajh.23357
文献    
  著者
Andolfo I, Alper SL, De Franceschi L, Auriemma C, Russo R, De Falco L, Vallefuoco F, Esposito MR, Vandorpe DH, Shmukler BE, Narayan R, Montanaro D, D'Armiento M, Vetro A, Limongelli I, Zuffardi O, Glader BE, Schrier SL, Brugnara C, Stewart GW, Delaunay J, Iolascon A
  タイトル
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
  雑誌
Blood 121:3925-35, S1-12 (2013)
DOI:10.1182/blood-2013-02-482489
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