Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A case of concomitant Gilbert's syndrome and hereditary spherocytosis.

The Korean journal of hepatology - 1 Sept 2010

Lee Hee Jung, Moon Hee Seok, Lee Eaum Seok, Kim Seok Hyun, Sung Jae Kyu, Lee Byung Seok, Jeong Hyun Yong, Lee Heon Young, Eu Young Jae

Abstract excerpt

We describe moderate hyperbilirubinemia in a 28-year-old man who suffered from gallstones and splenomegaly, with combined disorders of hereditary spherocytosis (HS) and Gilbert's syndrome (GS). Since it is difficult to diagnose HS in the absence of signs of anemia, we evaluated both the genetic mutation in the UGT1A1 gene and abnormalities in the erythrocyte membrane protein; the former was heterozygous for a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Ankyrins
Share to Electrophoresis, Polyacrylamide Gel

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gallstones

Share to Gilbert Disease

Share to Glucuronosyltransferase

Share to Protein Structure, Tertiary

Share to Spherocytosis, Hereditary

Share to Splenomegaly

Source

Open in PubMed Open full text

Identifiers

PMID: 20924216
DOI: 10.3350/kjhep.2010.16.3.321
PMCID: PMC3304593

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of concomitant Gilbert's syndrome and hereditary spherocytosis.PMID 20924216Read ↗

Genetic diagnosis and pathogenic analysis of an atypical hereditary spherocytosis combined with UGT1A1 partial deficiency: A case report.Semantic proximity Read ↗

A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome.Semantic proximity Read ↗

A Case of hereditary spherocytosis coexisting with Gilbert's syndrome.Semantic proximity Read ↗

[Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia].Semantic proximity Read ↗

[Analysis of diagnostic value of UGT1A1 gene detection in Gilbert syndrome].Semantic proximity Read ↗

Severe hyperbilirubinemia in a 10-year-old girl with a combined disorder of hereditary spherocytosis and Gilbert syndrome.Semantic proximity Read ↗

Coinheritance of Gilbert Syndrome Increases the Risk for Developing Gallstones in Patients With Hereditary SpherocytosisSemantic proximity Read ↗

Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.Semantic proximity Read ↗

A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report.Semantic proximity Read ↗

Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia.Semantic proximity Read ↗

Excessive bilirubin elevation in a patient with hereditary spherocytosis and intrahepatic cholestasis.Semantic proximity Read ↗

[Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.