Article
Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children.
Molecular genetics & genomic medicine - 1 Mar 2026
Li Yuzhuopu, Wang Yang, Liu Tao, Xiao Li, Huang Lan, Zhang Yongjie, Xiang Yan, Yu Jie
Abstract excerpt
BACKGROUND AND AIM: Hereditary spherocytosis (HS) is a common disease in hereditary hemolytic anemia. Advancements in sequencing technology have enabled the identification of a growing number of mutation sites associated with HS. This study analyzed the clinical characteristics and gene mutations of HS in our center. METHODS: Retrospective collection of data on 59 Chinese pediatric patients with HS admitted to...
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