Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males

Glucose‐6‐phosphate (G6PD) deficiency is the most common human enzyme defect, often presenting with neonatal jaundice and/or acute hemolytic anemia, triggered by oxidizing agents. G6PD deficiency is an X‐linked, hereditary disease, mainly affecting men, but should also be considered in females with...

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Detalles Bibliográficos
Autores principales: van den Broek, Leonie, Heylen, Evelien, van den Akker, Machiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134135/
https://www.ncbi.nlm.nih.gov/pubmed/27980749
http://dx.doi.org/10.1002/ccr3.714
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author van den Broek, Leonie
Heylen, Evelien
van den Akker, Machiel
author_facet van den Broek, Leonie
Heylen, Evelien
van den Akker, Machiel
author_sort van den Broek, Leonie
collection PubMed
description Glucose‐6‐phosphate (G6PD) deficiency is the most common human enzyme defect, often presenting with neonatal jaundice and/or acute hemolytic anemia, triggered by oxidizing agents. G6PD deficiency is an X‐linked, hereditary disease, mainly affecting men, but should also be considered in females with an oxidative hemolysis.
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spelling pubmed-51341352016-12-15 Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males van den Broek, Leonie Heylen, Evelien van den Akker, Machiel Clin Case Rep Case Reports Glucose‐6‐phosphate (G6PD) deficiency is the most common human enzyme defect, often presenting with neonatal jaundice and/or acute hemolytic anemia, triggered by oxidizing agents. G6PD deficiency is an X‐linked, hereditary disease, mainly affecting men, but should also be considered in females with an oxidative hemolysis. John Wiley and Sons Inc. 2016-10-24 /pmc/articles/PMC5134135/ /pubmed/27980749 http://dx.doi.org/10.1002/ccr3.714 Text en © 2016 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
van den Broek, Leonie
Heylen, Evelien
van den Akker, Machiel
Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males
title Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males
title_full Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males
title_fullStr Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males
title_full_unstemmed Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males
title_short Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males
title_sort glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134135/
https://www.ncbi.nlm.nih.gov/pubmed/27980749
http://dx.doi.org/10.1002/ccr3.714
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AT vandenakkermachiel glucose6phosphatedehydrogenasedeficiencynotexclusivelyinmales

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