G6PD Deficiency and Harilaou Variant in a Newborn: Intrauterine Haemolysis and Meconium Aspiration Syndrome

G6PD deficiency is one of the most commonly inherited enzymopathies with a hallmark of an X-linked pattern. G6PD has more than 300 unique variants with different enzyme activity. The G6PD Mediterranean variant is prevalent in Greece and associated with asymptomatic patients who may experience haemol...

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Detalles Bibliográficos
Autores principales: Athanasiadou, Kleoniki I., Amarantidou, Maria, Drogouti, Eftychia, Economou, Marina, Mitsiakos, George, Papakonstantinou, Evgenia, Karagianni, Paraskevi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2021
Materias:
Clinical Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603846/
https://www.ncbi.nlm.nih.gov/pubmed/34643346
http://dx.doi.org/10.34763/jmotherandchild.20212501.d-20-00021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603846/
https://www.ncbi.nlm.nih.gov/pubmed/34643346
http://dx.doi.org/10.34763/jmotherandchild.20212501.d-20-00021

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