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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Detalhes bibliográficos

Principais autores:	Xiaoyan LI, Xiaoli LAI, Dan WANG, Lina ZHANG, Xuan ZENG
Formato:	Artigo
Idioma:	Chinês
Publicado em:	Institute of Blood Transfusion of Chinese Academy of Medical Sciences 2022-03-01
Colecção:	Zhongguo shuxue zazhi
Assuntos:	pyruvate kinase deficiency pklr gene mn neonatal hemolytic disease
Acesso em linha:	https://www.cjbt.cn/thesisDetails#10.13303/j.cjbt.issn.1004-549x.2022.03.004&lang=en
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