Genetic diagnosis of MN and ABO hemolytic disease of the newborn complicated with pyruvate kinase deficiency: a case report and literature review
Objective To investigate the clinical and genetic characteristics of hemolytic disease of the newborn(HDN) induced by anti-M complicated with pyruvate kinase deficiency (PKD) disease. Methods The clinical data of a pregnant woman with unexplained adverse pregnancy outcome in the third trimester were...
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| Principais autores: | , , , , |
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| פורמט: | Artigo |
| שפה: | Chinês |
| יצא לאור: |
Institute of Blood Transfusion of Chinese Academy of Medical Sciences
2022-03-01
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| סדרה: | Zhongguo shuxue zazhi |
| נושאים: | |
| גישה מקוונת: | https://www.cjbt.cn/thesisDetails#10.13303/j.cjbt.issn.1004-549x.2022.03.004&lang=en |
| תגים: |
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