KEGG   DISEASE: Familial pseudohyperkalemia
Entry
H02001                      Disease                                
Name
Familial pseudohyperkalemia
  Supergrp
Hereditary stomatocytosis [DS:H00232]
Description
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.
Category
Hematologic disease
Brite
Human diseases in ICD-11 classification [BR:br08403]
 03 Diseases of the blood or blood-forming organs
  Anaemias or other erythrocyte disorders
   Haemolytic anaemias
    Congenital haemolytic anaemia
     3A10  Hereditary haemolytic anaemia
      H02001  Familial pseudohyperkalemia
Pathway
hsa02010  ABC transporters
Gene
(PSHK1) PIEZO1 [HSA:9780] [KO:K22128]
(PSHK2) ABCB6 [HSA:10058] [KO:K05661]
Other DBs
ICD-11: 3A10.3
MeSH: C563785
OMIM: 194380 609153
Reference
  Authors
Gore DM, Chetty MC, Fisher J, Nicolaou A, Stewart GW
  Title
Familial pseudohyperkalaemia Cardiff: a mild version of cryohydrocytosis.
  Journal
Br J Haematol 117:212-4 (2002)
DOI:10.1046/j.1365-2141.2002.03376.x
Reference
  Authors
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
  Title
Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.
  Journal
Am J Hematol 88:66-72 (2013)
DOI:10.1002/ajh.23357
Reference
  Authors
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
  Title
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
  Journal
Blood 121:3925-35, S1-12 (2013)
DOI:10.1182/blood-2013-02-482489
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