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

• Hoofdauteurs: Yafeng Wang (Auteur), Linlin Liu (Auteur), Dandan Liu (Auteur), Wei Liu (Auteur)
• Formaat: Boek
• Gepubliceerd in: BMC, 2023-05-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

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...