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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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| Yayımlandı: | Clin Case Rep |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5134135/ https://ncbi.nlm.nih.gov/pubmed/27980749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.714 |
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