G6PD deficiency and Harilaou variant in a newborn: Intrauterine haemolysis and meconium aspiration syndrome
Authors
2nd Neonatal Department and Neonatal Intensive Care Unit (NICU), Aristotle University of Thessaloniki, Papageorgiou General Hospital, Thessaloniki, Greece
2nd Neonatal Department and Neonatal Intensive Care Unit (NICU), Aristotle University of Thessaloniki, Papageorgiou General Hospital, Thessaloniki, Greece
2nd Neonatal Department and Neonatal Intensive Care Unit (NICU), Aristotle University of Thessaloniki, Papageorgiou General Hospital, Thessaloniki, Greece
1st Department of Pediatrics, Aristotle University of Thessaloniki, Hippokration General Hospital, Thessaloniki, Greece
2nd Neonatal Department and Neonatal Intensive Care Unit (NICU), Aristotle University of Thessaloniki, Papageorgiou General Hospital, Thessaloniki, Greece
Pediatric Oncology Department, Hippokration Hospital, Thessaloniki, Greece
2nd Neonatal Department and Neonatal Intensive Care Unit (NICU), Aristotle University of Thessaloniki, Papageorgiou General Hospital, Thessaloniki, Greece
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
Accepted on: Mar 25, 2021
Published on: Oct 11, 2021
Published by: Institute of Mother and Child
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
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© 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.