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

Case report: Dental management of Berardinelli-Seip congenital lipodystrophy.

European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry - 1 Apr 2016

Bhujel N, Clark H

Abstract excerpt

BACKGROUND: Berardinelli-Seip congenital lipodystrophy (BSCL) is a very rare autosomal recessive condition caused by mutations of the AGPAT2 gene or the BSCL2 gene. BSCL is associated with a number of dental manifestations. There are no published case reports of dental treatment under general anaesthesia (GA) in patients with this condition. CASE REPORT: A 6-year-old girl with BSCL characterised by classical...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to BSCL2 gene
Share to Malocclusion

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Source

Identifiers

PMID: 26573975
DOI: 10.1007/s40368-015-0210-z

Genes

AGPAT2
BSCL2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Case report: Dental management of Berardinelli-Seip congenital lipodystrophy.PMID 26573975Read ↗

Cherubism: best clinical practice.Semantic proximity Read ↗

[Radiographic findings in a case of congenital generalized lipodystrophy].Semantic proximity Read ↗

Berardinelli-Seip congenital lipodystrophy.Semantic proximity Read ↗

Cherubism—clinical picture and treatmentSemantic proximity Read ↗

Dentofacial Findings and Management of two Pediatric Patients With Bainbridge-Ropers Syndrome: A Case Report.Semantic proximity Read ↗

AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndrome.Semantic proximity Read ↗

Case Report: Holistic dental care for a child with Hunter syndrome: Addressing dental ramifications, overcoming challenges, and enhancing quality of lifeSemantic proximity Read ↗

Craniofacial and Dental Manifestations of Proteus Syndrome: A Case ReportSemantic proximity Read ↗

Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome.Semantic proximity Read ↗

Thalassaemia - part 1: a clinical update for the dental team.Semantic proximity Read ↗

General anesthesia in a patient with Hutchinson-Gilford progeria syndrome: two cases report of dental treatment in the one patientSemantic proximity Read ↗

Case Report: Dentigerous cyst marsupialization for a child with Hunter’s syndromeSemantic proximity Read ↗

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