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Updated: May 2, 2026

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
G6PD Enzyme Deficiency in Neonatal Pathologic Hyperbilirubinemia in Yazd
M Pahlavanzadeh1, S Hekmatimoghaddam2, M Teremahi Ardestani3
1Doctor of Laboratory Sciences, School of Paramedicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
Insights
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is prevalent in Iranian neonates with jaundice, with 18.1% affected. Early G6PD testing is recommended to prevent complications like hemolysis.
Area of Science:
- Medical Genetics
- Neonatology
- Biochemistry
Background:
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency affects 7.5% globally, with 10-14.9% prevalence in Iran.
- This genetic disorder is a significant public health concern, particularly in regions with high carrier rates.
Purpose of the Study:
- To determine the frequency of G6PD deficiency in jaundiced neonates hospitalized in Yazd, Iran.
- To assess the association between G6PD deficiency and the severity of neonatal jaundice.
Main Methods:
- A cohort of 105 icteric neonates was evaluated in Yazd hospitals.
- G6PD activity was measured using a photometric biochemical assay.
- Statistical analysis included Student's t-test and Pearson's chi-squared test.
Main Results:
- 18.1% of neonates (19 out of 105) exhibited G6PD deficiency, with a higher prevalence in boys (29.4%) than girls (7.4%).
- Jaundice onset occurred within the first week of life in all cases.
- G6PD-deficient neonates required exchange transfusion significantly more often (31.5%) compared to G6PD-sufficient neonates (4.6%).
Conclusions:
- The frequency of G6PD deficiency among jaundiced neonates in Yazd is notably high.
- Given the severity and increased need for intervention, screening all jaundiced neonates for G6PD is recommended.
- Universal G6PD testing in neonates is advised to prevent severe complications such as favism and drug-induced hemolysis.
Background:
About 7.5% of the world population carries one or two deficient copy of glucose-6-phosphate dehydrogenase (G6PD) genes. According to WHO, its prevalence in Iran is 10 to 14.9%. This study aimed on determination of frequency of G6PD deficiency in neonates with jaundice who were hospitalized during 6 months (September 2008 to February 2009) in the city of Yazd, Iran.
Materials And Methods:
In this study, 105 icteric neonates in the hospitals of Yazd were evaluated. Data was collected from hospital records, and the G6PD activity was measured by photometric biochemical assay. Statistical analysis of data was performed by the SPSS-16 software, using Student's t-test and Pearson's chi-squared test.
Results:
Between all of studied neonates, 19 (18.1%) had G6PD deficiency, and consisted of 15 boys (29.4% of boys) and 4 girls (7.4% of girls). In 100% of cases, the jaundice began in the first week after birth. The average total serum bilirubin at hospitalization was 17.22 mg/dL. In 31.5% of the G6PD-defficient neonates, exchange transfusion became necessary, which is significantly more than the rate in G6PD-sufficient (4.6%) neonates (P-value<0.05).
Conclusion:
In general, the frequency of G6PD deficiency in this study seems quite high. Regarding its severity and frequent need for exchange transfusion, we recommend that all of the icteric neonates should be evaluated for G6PD activity. Also, it is better to test for G6PD deficiency in all of the neonates, to detect its presence and to prevent its complications such as favism and oxidant drug-induced hemolysis, since the test has a low cost.
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