A literature review and case report of severe hepatitis caused by the G6PD gene c.1478G>A muta-tion
G6PD (glucose-6-phosphate dehydrogenase) deficiency is the most common enzyme deficiency disease in humans affecting over 500 million people worldwide, with most patients being children aged 2 to 10 years. G6PD deficiency usually has an acute onset and manifests as acute hemolytic anemia. Clinically...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | zho |
| Published: |
Editorial Office of New Medicine
2021-08-01
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| Series: | Yixue xinzhi zazhi |
| Subjects: | |
| Online Access: | https://yxxz.whuznhmedj.com/storage/attach/2108/tq0SDj7TTwgqwFKcFvjTnuLZNQTCAQigeFd7rJsI.pdf |
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