Familial Partial Lipodystrophy | List of Frontiers open access articles

Mini Review

Published on 09 Jul 2018

Lamin A, Chromatin and FPLD2: Not Just a Peripheral Ménage-à-Trois

in Epigenomics and Epigenetics

Nolwenn Briand
Inswasti Cahyani
Julia Madsen-Østerbye
Jonas Paulsen
Torunn Rønningen
Anita L. Sørensen
Philippe Collas

Frontiers in Cell and Developmental Biology

doi 10.3389/fcell.2018.00073

6,738 views
5 citations

Case Report

Published on 08 Jun 2021

Case Report: Metreleptin Treatment in a Patient With a Novel Mutation for Familial Partial Lipodystrophy Type 3, Presenting With Uncontrolled Diabetes and Insulin Resistance

in Obesity

Vaia Lambadiari
Aikaterini Kountouri
Eirini Maratou
Stavros Liatis
George D. Dimitriadis
Fredrik Karpe

Frontiers in Endocrinology

doi 10.3389/fendo.2021.684182

6,394 views
15 citations

Case Report

Published on 29 Mar 2022

Case Report: A New Peroxisome Proliferator-Activated Receptor Gamma Mutation Causes Familial Partial Lipodystrophy Type 3 in a Chinese Patient

in Obesity

Xi Chen
Zhiqiang Ma
Peng Chen
Xiuli Song
Weihua Li
Xuefeng Yu
Junhui Xie

Frontiers in Endocrinology

doi 10.3389/fendo.2022.830708

4,012 views
11 citations

Original Research

Published on 03 Jun 2024

Comprehensive analysis of morbidity and mortality patterns in familial partial lipodystrophy patients: insights from a population study

in Clinical Diabetes

Natália Rossin Guidorizzi
Cynthia M. Valerio
Luiz F. Viola
Victor Rezende Veras
Virgínia Oliveira Fernandes
Grayce Ellen da Cruz Paiva Lima
Amanda Caboclo Flor
Jessica Silveira Araújo
Raquel Beatriz Gonçalves Muniz
Rodrigo Oliveira Moreira

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1359211

4,555 views
10 citations

Review

Published on 27 Sep 2024

Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features

in Clinical Diabetes

Reivla Marques Vasconcelos Soares
Monique Alvares da Silva
Julliane Tamara Araújo de Melo Campos
Josivan Gomes Lima

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1394102

5,155 views
8 citations

Case Report

Accepted on 26 Jan 2026

Familial partial lipodystrophy: description of novel and ultrarare variants with distinct phenotypic spectrum

in Obesity

Silvia Magno
Caterina Pelosini
Melania Paoli
Donatella Gilio
Lavinia Palladino
Francesca Menconi
Andrea Barison
Barbara Coco
Giordano Paolucci
Guido Salvetti

Frontiers in Endocrinology

127 views

Case Report

Published on 19 Apr 2021

Case Report: An Atypical Form of Familial Partial Lipodystrophy Type 2 Due to Mutation in the Rod Domain of Lamin A/C

in Obesity

Carolina Cecchetti
M. Rosaria D’Apice
Elena Morini
Giuseppe Novelli
Carmine Pizzi
Uberto Pagotto
Alessandra Gambineri

Frontiers in Endocrinology

doi 10.3389/fendo.2021.675096

5,451 views
5 citations

Original Research

Published on 21 May 2025

A real-world pharmacovigilance assessment and literature review of lymphoma development in lipodystrophy

in Cancer Endocrinology

Rebecca J. Brown
David Araujo-Vilar
Kelly J. Walkovich
Alexandru Barbarosie
David A. Magee
Baris Akinci
Elif A. Oral

Frontiers in Endocrinology

doi 10.3389/fendo.2025.1582715

4,741 views
1 citation

Original Research

Published on 03 Apr 2024

Gestational and neonatal outcomes of women with partial Dunnigan lipodystrophy

in Clinical Diabetes

Cynthia M. Valerio
Raquel Beatriz Gonçalves Muniz
Luiz F. Viola
Gabriela Bartzen Pereira
Rodrigo Oliveira Moreira
Marise Ribeiro de Sousa Berriel
Renan Magalhães Montenegro Júnior
Amélio F. Godoy-Matos
Lenita Zajdenverg

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1359025

4,469 views
4 citations

Case Report

Published on 28 Nov 2024

Case Report: Concurrent de novo pathogenic variants in the LMNA gene as a cause of sporadic partial lipodystrophy

in Genetics of Common and Rare Diseases

José L. Santos
José Patricio Miranda
Carlos F. Lagos
Víctor A. Cortés

Frontiers in Genetics

doi 10.3389/fgene.2024.1468878

3,678 views
2 citations

Correction

Published on 03 Dec 2024

Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features

in Clinical Diabetes

Reivla Marques Vasconcelos Soares
Monique Alvares da Silva
Julliane Tamara Araújo de Melo Campos
Josivan Gomes Lima

Frontiers in Endocrinology

doi 10.3389/fendo.2024.1508146

1,063 views
2 citations

Original Research

Published on 15 Jun 2017

LMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 Diabetes

in Epigenomics and Epigenetics

Alyssa Florwick
Tejas Dharmaraj
Julie Jurgens
David Valle
Katherine L. Wilson

Frontiers in Genetics

doi 10.3389/fgene.2017.00079

14,408 views
23 citations

Articles

Lamin A, Chromatin and FPLD2: Not Just a Peripheral Ménage-à-Trois

Case Report: Metreleptin Treatment in a Patient With a Novel Mutation for Familial Partial Lipodystrophy Type 3, Presenting With Uncontrolled Diabetes and Insulin Resistance

Case Report: A New Peroxisome Proliferator-Activated Receptor Gamma Mutation Causes Familial Partial Lipodystrophy Type 3 in a Chinese Patient

Comprehensive analysis of morbidity and mortality patterns in familial partial lipodystrophy patients: insights from a population study

Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features

Familial partial lipodystrophy: description of novel and ultrarare variants with distinct phenotypic spectrum

Case Report: An Atypical Form of Familial Partial Lipodystrophy Type 2 Due to Mutation in the Rod Domain of Lamin A/C

A real-world pharmacovigilance assessment and literature review of lymphoma development in lipodystrophy

Gestational and neonatal outcomes of women with partial Dunnigan lipodystrophy

Case Report: Concurrent de novo pathogenic variants in the LMNA gene as a cause of sporadic partial lipodystrophy

Corrigendum: Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features

LMNA Sequences of 60,706 Unrelated Individuals Reveal 132 Novel Missense Variants in A-Type Lamins and Suggest a Link between Variant p.G602S and Type 2 Diabetes