Exchange Transfussion for the Treatment of Severe Indirect Hyperbilirubinemia Caused by Glucose-6-Phosphate Dehydrogenase Deficiency: A Case Report
Hyperbilirubinemia is a common problem during the neonatal period, which can lead to high morbidity and mortality if it is not treated properly. The most common first-line treatment used for hyperbilirubinemia is phototherapy. Glucose-6-phosphate dehydrogenase deficiency (G6PD) can cause indirect hyperbilirubinemia not only with hemolysis but also by affecting bilirubin metabolism in the liver during the neonatal period. In here, we report a three-day-old newborn with severe hyperbilirubinemia who underwent exchange transfusion with a diagnosis of G6PD deficiency to emphasize the importance of keeping in mind erythtocyte enzyme defects in the differential diagnosis of severe indirect hyperbilirubinemia.
Authors
- Erbu Yarcı (ORCID: https://orcid.org/0000-0003-4434-0958)
- Bayram Ali̇ Dorum (ORCID: https://orcid.org/0000-0002-2823-8454)
- Hatice Buket Özay (ORCID: https://orcid.org/0000-0003-2649-9527)
- Melek Tandoğan
Institutions
- Bursa Technical University (TR)
- Sağlık Bilimleri Üniversitesi (TR)
- University of Health Sciences Antigua (AG)
Publication Details
- Journal
- Fetal and Pediatric Pathology
- Published
- 2025-09-27
- DOI
- https://doi.org/10.1080/15513815.2025.2565690
- Primary Topic
- Neonatal Health and Biochemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00