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Article

Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II).

The Journal of pediatrics - 1 Apr 2000

Perrotta S, del Giudice E M, Carbone R, Servedio V, Schettini F, Nobili B, Iolascon A

Abstract excerpt

The molecular basis for the considerable variation of serum bilirubin levels and the incidence of gallstone formation in patients with congenital dyserythropoietic anemia (CDA) type II are unknown. We show that the combined effect of an increased bilirubin load caused by dyserythropoiesis in CDA...

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Source

Identifiers

PMID: 10753261
DOI: 10.1016/s0022-3476(00)90026-x

Genes

CDA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10753261-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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