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Gluthathione peroxidase deficiency(GPXD)

MedGen UID:
473098
Concept ID:
C0398747
Disease or Syndrome
Synonym: Glutathione peroxidase deficiency
SNOMED CT: Gluthathione peroxidase deficiency (234590006)
 
Gene (location): GPX1 (3p21.31)
 
Monarch Initiative: MONDO:0013601
OMIM®: 614164

Definition

Several documented cases of glutathione peroxidase (GPX1; 138320) deficiency in association with hemolytic anemia have been reported. However, Paglia (1989) stated: 'To date, no defects in glutathione peroxidase have been unequivocally incriminated in the pathogenesis of hemolytic syndromes, although several instances of partial deficiency have been reported in patients with anemias of unknown etiology. This association may be coincidental, since there is a broad range of ethnic variation in the erythrocyte enzyme' (Beutler and Matsumoto, 1975). [from OMIM]

Clinical features

From HPO
Heinz bodies
MedGen UID:
42375
Concept ID:
C0018871
Cell Component
A type of erythrocyte inclusion composed of denatured hemoglobin.
Compensated hemolytic anemia
MedGen UID:
870825
Concept ID:
C4025283
Disease or Syndrome
Neonatal hyperbilirubinemia
MedGen UID:
208991
Concept ID:
C0857007
Disease or Syndrome
A type of hyperbilirubinemia with neonatal onset.

Recent clinical studies

Clinical prediction guides

Bridi R, Latini A, Braum CA, Zorzi GK, Moacir W, Lissi E, Dutra-Filho CS
Free Radic Res 2005 Jan;39(1):71-9. doi: 10.1080/10715760400022350. PMID: 15875814

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