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Article

Hereditary spherocytosis in 3 children coexisting with UDP-glucuronyl transferase 1A1 deficiency.

Journal of pediatric hematology/oncology - 1 Feb 2009

Shiota Mitsutaka, Asada Junko, Nishida Hitoshi, Kumakura Akira, Yoshioka Takakazu, Hata Atsuko, Watanabe Ken, Maruo Yoshihiro, Kato Junko, Ideguchi Hiroshi, Nakanishi Hidekazu, Sugihara Takashi, Hata Daisuke

Abstract excerpt

Simultaneous presence of hemolytic anemia and bilirubin UDP-glucuronosyltransferase deficiency is a possible cause of misdiagnosis. Seven-year-old and 17-year-old brothers and a 15-year-old sister consecutively suffered from aplastic crises. Although few spherocytes were present, the siblings and their mother had diagnoses of hereditary spherocytosis with flow cytometric analysis of eosin-5'-maleimide-labeled red...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19194197
DOI: 10.1097/MPH.0b013e318190d9cf

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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