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Article

Persistent jaundice in an infant with homozygous beta thalassemia due to co-inherited Crigler-Najjar syndrome.

Pediatric blood & cancer - 1 Apr 2010

Aggarwal Varun, Seth Anju, Sharma Sunita, Aneja Satinder, Sammarco Pietro, Fabiano Carmelo

Abstract excerpt

Clinically apparent jaundice is unusual in patients with beta-thalassemia major. Co-inheritance of Gilbert syndrome has been reported to cause hyperbilirubinemia in these subjects. Crigler-Najjar syndrome is another rare disorder of bilirubin metabolism caused by mutation in the gene coding the e...

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Source

Identifiers

PMID: 19953640
DOI: 10.1002/pbc.22313

Genes

AGT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19953640-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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