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

Obstructive sleep apnea in familial partial lipodystrophy type 2 with atypical skin findings and vascular disease.

Sleep & breathing = Schlaf & Atmung - 1 Nov 2009

Patel Kumar, Roseman Debra, Burbank Heather, Attarian Hrayr

Abstract excerpt

INTRODUCTION: A number of metabolic conditions have been associated with Obstructive Sleep Apnea Syndrome (OSAS). Familial partial lipodystrophy type 2 (FPLD2), one of the few rare genetic disorders affecting total body fat redistribution, is one of those conditions. CASE REPORT: In this case rep...

Read the complete abstract on PubMed

Topics

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

Share to Arousal
Share to Body Fat Distribution
Share to Carotid Stenosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lamin Type A

Share to Lipodystrophy, Familial Partial

Share to Polysomnography

Share to Skin Diseases, Genetic

Share to Sleep Apnea, Obstructive

Source

Identifiers

PMID: 19418082
DOI: 10.1007/s11325-009-0261-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19418082-2026-09-02.2. 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

Obstructive sleep apnea in familial partial lipodystrophy type 2 with atypical skin findings and vascular disease.PMID 19418082Read ↗

Clinical review#: Lipodystrophies: genetic and acquired body fat disorders.Semantic proximity Read ↗

Multiple symmetric and multiple familial lipomatosis.Semantic proximity Read ↗

Obstructive sleep apnea in 2 women with familial partial lipodystrophy due to a heterozygous LMNA R482Q mutation.Semantic proximity Read ↗

Multiple Symmetric Lipomatosis: New Classification System Based on the Largest German Patient CohortSemantic proximity Read ↗

Aldo-keto reductase 1C2 (AKR1C2) as the second gene associated to non-syndromic primary lipedema: investigating activating mutation or overexpression as causative factors.Semantic proximity Read ↗

Novel and Ultrarare Heterozygous Missense LMNA Variants Causing Familial Partial Lipodystrophy.Semantic proximity Read ↗

Sjögren-Larsson syndrome: phenotypic variability in two brothers with a neurocutaneous disorder.Semantic proximity Read ↗

[Benign symmetrical Launois-Bensaude type II lipomatosis with market systemic involvement and psoriasis].Semantic proximity Read ↗

Dunnigan-Kobberling syndrome: an autosomal dominant form of partial lipodystrophy.Semantic proximity Read ↗

Multiple Symmetrical Lipomatosis — A mitochondrial disorder of brown fatSemantic proximity Read ↗

Lipedema: an inherited condition.Semantic proximity Read ↗

Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy.Semantic proximity Read ↗

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