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 hereditary spherocytosis coexisting with Gilbert's syndrome.

The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi - 25 Mar 2013

Lee Min Jae, Chang Yoon Hwan, Kang Seung Hwa, Mun Se Kwon, Kim Heyjin, Han Chul Ju, Kim Jin, Kang Hye Jin

Abstract excerpt

We recently encountered a case of hereditary spherocytosis coexisting with Gilbert's syndrome. Patient was initially diagnosed with Gilbert's syndrome and observed, but other findings suggestive of concurrent hemolysis, such as splenomegaly and gallstones were noted during the follow-up period. T...

Read the complete abstract on PubMed

Topics

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

Share to Erythrocytes
Share to Gallstones
Share to Gilbert Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucuronosyltransferase

Share to Hemolysis

Share to Hyperbilirubinemia

Share to Spherocytosis, Hereditary

Share to Splenomegaly

Source

Identifiers

PMID: 23575236
DOI: 10.4166/kjg.2013.61.3.166

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23575236-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Case of hereditary spherocytosis coexisting with Gilbert's syndrome.PMID 23575236Read ↗

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

Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases.Semantic proximity Read ↗

A case of concomitant Gilbert's syndrome and hereditary spherocytosis.Semantic proximity Read ↗

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

[Gene mutation pattern of Gilbert's syndrome combined with viral hepatitis and its relationship with the exploration of clinical data].Semantic proximity Read ↗

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 ↗

"Gilbert's-like" syndrome as part of a spectrum of persistent unconjugated hyperbilirubinemia in post-chronic hepatitis patients.Semantic proximity Read ↗

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

[Repeated yellowing of the skin and sclera for 2 years].Semantic proximity Read ↗

Unusual Gilbert's syndrome genotype in a Greek patient suffering from both Gilbert's syndrome and familial mediterranean fever. A case report.Semantic proximity Read ↗

[Influence of Gilbert's syndrome on serum bilirubin levels and gallstone formation in children with chronic hemolytic disease].Semantic proximity Read ↗

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