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Article

Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophy.

The Journal of clinical endocrinology and metabolism - 1 Jun 2008

Vantyghem M C, Vincent-Desplanques D, Defrance-Faivre F, Capeau J, Fermon C, Valat A S, Lascols O, Hecart A C, Pigny P, Delemer B, Vigouroux C, Wemeau J L

Abstract excerpt

OBJECTIVE: Familial partial lipodystrophy due to LMNA (lamin A/C) mutations is a rare disorder characterized by a selective loss of adipose tissue and insulin resistance. Dyslipidemia and severe diabetes often occur during its evolution. Only isolated and contradictory case reports have been published on the obstetrical prognosis in lipodystrophy. The aim of our study was to compare the fertility and occurrence...

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

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Source

Identifiers

PMID: 18364375
DOI: 10.1210/jc.2007-2521

Genes

LMNA

Variants

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

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophy.PMID 18364375Read ↗

Advances in lipodystrophy syndrome caused by LMNA gene mutation.Semantic proximity Read ↗

[Biochemical, hormonal and genetic evaluation of the families of two Brazilian patients with type 2 familial partial lipodystrophy].Semantic proximity Read ↗

Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes.Semantic proximity Read ↗

Familial partial lipodystrophy associated with the heterozygous LMNA mutation 1445G>A (Arg482Gln) in a Polish family.Semantic proximity Read ↗

A novel autosomal recessive lipodystrophy syndrome due to homozygous LMNA variant.Semantic proximity Read ↗

Familial Generalized and Partial Lipodystrophies Due to Rare Biallelic Variants in LMNA.Semantic proximity Read ↗

The Clinical Characteristics and Potential Molecular Mechanism of LMNA Mutation-Related Lipodystrophy.Semantic proximity Read ↗

A recurrent familial partial lipodystrophy due to a monoallelic or biallelic LMNA founder variant highlights the multifaceted cardiac manifestations of metabolic laminopathies.Semantic proximity Read ↗

LMNA-associated partial lipodystrophy: anticipation of metabolic complications.Semantic proximity Read ↗

Podocytopathies associated with familial partial lipodystrophy due to LMNA variants: report of two cases.Semantic proximity Read ↗

Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation.Semantic proximity Read ↗

Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in the LMNA gene.Semantic proximity Read ↗

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