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DOI 10.19746/j.cnki.issn.1009-2137.2021.06.036

Медицинская библиотека · Zhongguo shi yan xue ye xue za zhi · 2021

[Hb Bart's Quantitative Analysis in the Screening of α-Thalassemia].

Yi Song, Wang Bo, Li Hui, Zhang Hao, Song Jie-Ping

СтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

To research the relationship between difference types of α-thalassemia gene types and Hb Bart's hemoglobin bands.

METHODS

Capillary electrophoresis was used to screen thalassemia gene for the newborn form January 2020 to December 2020, and the thalassemia gene was detected by PCR or PCR-NGS in the positive patients. The relationship between α-thalassemia gene and Hb Bart's hemoglobin was compared and analyzed statistically.

RESULTS

There were significant differences in Hb Bart's hemoglobin among the different α-thalassemia mutation types, Hb Bart's was the highest in --SEA/-α3.7 compound heterozygous mutation, then in --SEA/αα single heterozygous deletion type and in -α3.7/-α3.7,-α3.7/-α4.2compound heterozygous mutation, and in αqsα/αα, αcsα/αα single heterozygous point mutation, least in -α3.7/αα and -α4.2/αα single heterozygous deletion type. There were significant difference among the each groups.

CONCLUSION

The Hb Bart's content of different genotypes of α-thalassemia are significantly different. The Hb Bart's content shows high application value in α-thalassemia screening and genotyping identification.

Для цитирования: Yi Song, Wang Bo, Li Hui, Zhang Hao, Song Jie-Ping. [Hb Bart's Quantitative Analysis in the Screening of α-Thalassemia].. Zhongguo shi yan xue ye xue za zhi. 2021. DOI: 10.19746/j.cnki.issn.1009-2137.2021.06.036.

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