A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report

A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report

Abstract Background Due to the heterogeneity of the phenotype of Hereditary spherocytosis (HS) patients, some patients may have rare clinical complications such as biliary obstruction and ultra-high bilirubinemia. Case presentation A 8-y-old boy presented to the emergency with complaints of anemia f...

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Bibliographic Details
Main Authors: Yafeng Wang, Linlin Liu, Dandan Liu, Wei Liu
Format: Article
Language:English
Published: BMC 2023-05-01
Series:BMC Pediatrics
Subjects:
Hereditary spherocytosis
Children
ANK1
Mutation
Biliary obstruction
Online Access:https://doi.org/10.1186/s12887-023-04092-0

Internet

https://doi.org/10.1186/s12887-023-04092-0

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