Lanean...
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...
Gorde:
| Argitaratua izan da: | Clin Case Rep |
|---|---|
| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
John Wiley and Sons Inc.
2016
|
| Gaiak: | |
| Sarrera elektronikoa: | 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 |
| Etiketak: |
Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|