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G6PD deficiency and Harilaou variant in a newborn: Intrauterine haemolysis and meconium aspiration syndrome Cover

G6PD deficiency and Harilaou variant in a newborn: Intrauterine haemolysis and meconium aspiration syndrome

Open Access
|Oct 2021

Figures & Tables

Figure 1

Family pedigree
Family pedigree

WHO classification of G6PD variants according to the degree of enzyme deficiency and severity of haemolysis

Class ISevere enzyme deficiency (<1% residual activity) chronic non-spherocytic haemolysis
Class IISevere enzyme deficiency (1–10% residual activity) intermittent acute haemolysis
Class IIIModerate enzyme deficiency (10–60% residual activity) intermittent acute haemolysis
Class IVNo enzyme deficiency (60–150% activity)
Class VIncreased enzyme activity (>150%)
DOI: https://doi.org/10.34763/jmotherandchild.20212501.d-20-00021 | Journal eISSN: 2719-535X | Journal ISSN: 2719-6488
Language: English
Page range: 61 - 64
Submitted on: Dec 17, 2020
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Accepted on: Mar 25, 2021
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Published on: Oct 11, 2021
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2021 Kleoniki I. Athanasiadou, Maria Amarantidou, Eftychia Drogouti, Marina Economou, George Mitsiakos, Evgenia Papakonstantinou, Paraskevi Karagianni, published by Institute of Mother and Child
This work is licensed under the Creative Commons Attribution 4.0 License.