Haemolytic anaemia due to glutathione reductase deficiency (Q93776): Difference between revisions

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Latest revision as of 08:52, 16 August 2026

Haemolytic anaemia due to glutathione reductase (GSR) deficiency is characterised by nearly complete absence of GSR activity in erythrocytes. It has been described in three children (one male and two females) born to consanguineous parents. Both parents had intermediate levels of GSR activity. One child presented with favism and two with cataracts. Transmission is autosomal recessive. This disease should be distinguished from glutathione reductase deficiency secondary to dietary riboflavin deficiency and from the acute pharmacologic phenocopy induced by carmustine (BCNU). GSR activity is not restored by riboflavin in vivo or by FAD in vitro.

Language	Label	Description	Also known as
default for all languages	ID_286285535
English	Haemolytic anaemia due to glutathione reductase deficiency	Haemolytic anaemia due to glutathione reductase (GSR) deficiency is characterised by nearly complete absence of GSR activity in erythrocytes. It has been described in three children (one male and two females) born to consanguineous parents. Both parents had intermediate levels of GSR activity. One child presented with favism and two with cataracts. Transmission is autosomal recessive. This disease should be distinguished from glutathione reductase deficiency secondary to dietary riboflavin deficiency and from the acute pharmacologic phenocopy induced by carmustine (BCNU). GSR activity is not restored by riboflavin in vivo or by FAD in vitro.