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Article

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

BMC pediatrics - 29 May 2023

Wang Yafeng, Liu Linlin, Liu Dandan, Liu Wei

Abstract excerpt

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 for 6 years and worsened abdominal pain and scleral yellowing of the skin for 2 days. Physical examination showed tenderness...

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Identifiers

PMID: 37246216
DOI: 10.1186/s12887-023-04092-0
PMCID: PMC10226236

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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