Late-Life Presentation of Unsuspected G6PD Deficiency
Deficiency of glucose-6-phosphate dehydrogenase (G6PD) is the commonest enzyme deficiency in humans with a wide range of possible clinical manifestations depending on the specific genetic variant in each case. Here we present the case of an 86-year-old male of African descent who acutely developed s...
| Hlavní autoři: | , , |
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| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
Hindawi Limited
2018-01-01
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| Edice: | Case Reports in Critical Care |
| On-line přístup: | http://dx.doi.org/10.1155/2018/8198565 |