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Prevalence of G6PD deficiency in Children with Hepatitis A
Ghasem Miri-Aliabad1, Ali Khajeh2, Tooran Shahraki2
1Assistant Professor of Pediatric Hematology-Oncology, Children and Adolescent Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran.
Insights
Hepatitis A is common, and this study found a high prevalence of glucose 6-phosphate dehydrogenase (G6PD) deficiency in children with this infection. Testing for G6PD deficiency is recommended in endemic areas.
Area of Science:
- Pediatrics
- Hepatology
- Hematology
Background:
- Hepatitis A virus (HAV) is a leading cause of viral hepatitis globally.
- Clinical presentations of HAV infection vary widely.
- Glucose 6-phosphate dehydrogenase (G6PD) deficiency is a common inherited enzyme disorder.
Purpose of the Study:
- To investigate clinical findings in children diagnosed with Hepatitis A.
- To determine the prevalence of G6PD deficiency among pediatric Hepatitis A patients.
Main Methods:
- Prospective study design.
- Inclusion of 117 children with Hepatitis A confirmed by anti-HAV IgM antibody.
- Measurement of G6PD enzyme activity using the fluorescent spot test.
Main Results:
- The majority of patients (55.6%) were female, with a mean age of 2.79 years.
- Common symptoms included dark yellow urine and anorexia.
- G6PD deficiency was identified in 26.3% of tested pediatric patients.
Conclusions:
- High prevalence of G6PD deficiency in pediatric Hepatitis A cases suggests a need for routine screening.
- Recommendations include measuring G6PD levels alongside liver function tests in endemic regions.
- Close monitoring for hemolysis and renal function is advised for these patients.
Abstract:
Introduction: Hepatitis A virus is the most prevalent viral hepatitis. It is globally a major public health problem with different clinical symptoms. This study aimed at investigating the clinical findings and prevalence of glucose 6-phosphate dehydrogenase (G6PD) deficiency in children with hepatitis A. Materials and Methods: In this prospective study, demographical information, clinical findings, and G6PD level of hepatitis A patients, who were visited at Pediatric Hematology clinic, were entered into the database. The diagnosis of hepatitis A infection was based on the presence of anti-HAV IgM antibody. The activity of G6PD enzyme was measured with florescent spot test. Results: Of the 117 children with hepatitis A, 52 (44.4%) were male and 65 (55.6%) were female. The mean age of these patients was 2.79±5.39 years. The most prevalent clinical manifestations were dark yellow urine and anorexia. G6PD deficiency was observed in 26 (26.3%) out of 99 patients whose G6PD levels were measured. Conclusion: Given the high prevalence of G6PD deficiency in this study, the measurement of G6PD level along with other liver and biochemical markers in areas with endemic hepatitis A is recommended. In addition, it is recommended that patients undertake precise monitoring for hemolysis and renal function.
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