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

[Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases].

La Tunisie medicale - 1 Oct 2010

Aloulou Hajer, Ben Thabet Afef, Khanfir Sonia, Ben Mansour Lamia, Chabchoub Imen, Labrune Phillipe, Kammoun Thouraya, Hachicha Mongia

Abstract excerpt

BACKGROUND: Crigler-Najjar syndrome is a rare metabolic disorder characterized by severe unconjugated hyperbilirubinemia resulting in deficiency of bilirubin uridine diphosphate (UDP) glucuronosyltransferase activity in the liver. AIM: To study the clinical, genetic therapeutic aspects and the ou...

Read the complete abstract on PubMed

Topics

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

Share to Crigler-Najjar Syndrome
Share to Glucuronosyltransferase
Share to Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Mutation

Share to Tunisia

Source

Identifiers

PMID: 20890816

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20890816-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases].PMID 20890816Read ↗

Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect.Semantic proximity Read ↗

Therapeutic Options for Crigler-Najjar Syndrome: A Scoping ReviewSemantic proximity Read ↗

Crigler-Najjar syndrome type 2.Semantic proximity Read ↗

UGT1A1 gene mutation due to Crigler-Najjar syndrome in Iranian patients: identification of a novel mutation.Semantic proximity Read ↗

Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia.Semantic proximity Read ↗

[Genetic analysis of a child affected with Crigler-Najjar syndrome type II].Semantic proximity Read ↗

Crigler-Najjar Syndrome: Current Perspectives and the Application of Clinical GeneticsSemantic proximity Read ↗

Identification of three novel variants in the UGT1A1 gene as a cause of Crigler-Najjar syndrome type 1Semantic proximity Read ↗

The Tunisian population history through the Crigler-Najjar type I syndrome.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 ↗

Genetic diseases in the Tunisian population.Semantic proximity Read ↗

Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family.Semantic proximity Read ↗

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