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Article

Recurrent familial intrahepatic cholestasis in the Faeroe Islands. Phenotypic heterogeneity but genetic homogeneity.

Hepatology (Baltimore, Md.) - 1 Feb 1999

Tygstrup N, Steig B A, Juijn J A, Bull L N, Houwen R H

Abstract excerpt

Recurrent familial intrahepatic cholestasis is an autosomal recessive disorder characterized by episodes of severe pruritus and jaundice lasting for weeks to months without extrahepatic bile duct obstruction. Symptom-free intervals may last for months to years, and chronic liver damage does not d...

Topics

Adenosine Triphosphatases
Adult
Aging
Cholestasis, Intrahepatic
Denmark
Female
Genotype
Humans
Male
Middle Aged
Mutation
Phenotype
Recurrence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 9918928
DOI: 10.1002/hep.510290214

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9918928-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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