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Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.

Bailliere's best practice & research. Clinical haematology - 1 Mar 2000

Fiorelli G, Martinez di Montemuros F, Cappellini M D

Abstract excerpt

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being present in over 400 million people world wide. In a small number of cases, G6PD deficiency can lead to mild-to-severe chronic haemolysis, which is further exacerbated by oxidative stress. Such G6PD variants have been described all over the world and are responsible for chronic non-spherocytic haemolytic anaemia...

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Identifiers

PMID: 10916677
DOI: 10.1053/beha.1999.0056

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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