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Hematology Volume 27, 2022 - Issue 1
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Case Report

The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review

Li Dua Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
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Danqing Qina Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
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Jicheng Wanga Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
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Cuize Yaoa Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
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Juan Zhua Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
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Hao Guoa Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
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Tenglong Yuana Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
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Jie Lianga Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaView further author information
&
Aihua Yina Medical Genetic Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;b Maternal and Children Metabolic-Genetic Key Laboratory, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of China;c Thalassemia Diagnosis Center, Guangdong Women and Children Hospital, Guangzhou, People’s Republic of ChinaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0001-9498-9777View further author information
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Pages 258-262 | Published online: 22 Feb 2022

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