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Hemoglobin
international journal for hemoglobin research
Volume 46, 2022 - Issue 6
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Brief Reports

Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report

Shao-Min Wua Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, Guangdong Province, People’s Republic of ChinaView further author information
,
Su-Ran Huanga Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, Guangdong Province, People’s Republic of ChinaView further author information
,
Chan Lia Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, Guangdong Province, People’s Republic of ChinaView further author information
,
Gui-Lan Chenb Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of ChinaView further author information
&
Dong-Zhi Lib Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of ChinaCorrespondence[email protected]
View further author information
Pages 341-343 | Received 15 Nov 2022, Accepted 22 Dec 2022, Published online: 23 Feb 2023

References

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  • Pedroso GA, Kimura EM, Santos MNN, et al. Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly>Arg (HBA2:C.178G>C)] in a Brazilian child. Pediatr Blood Cancer. 2018;65(12):e27413.
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  • Jiang F, Zuo L, Li J, et al. Evaluation of intervention strategy of thalassemia for couples of childbearing ages in Centre of Southern China. J Clin Lab Anal. 2021;35(10):e23990.

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