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Article

Neonatal screening for glucose-6-phosphate dehydrogenase deficiency: biochemical versus genetic technologies.

Seminars in perinatology - 1 Jun 2011

Kaplan Michael, Hammerman Cathy

Abstract excerpt

Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency, a commonly occurring genetic condition, is associated in neonates with severe hemolytic episodes, extreme hyperbilirubinemia, and bilirubin encephalopathy. Neonatal screening programs for the condition should increase parental and caretaker a...

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Identifiers

PMID: 21641489
DOI: 10.1053/j.semperi.2011.02.010

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21641489-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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