Partial Lipodystrophy | List of Frontiers open access articles

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

3,673 views
2 citations

Original Research

Published on 16 Nov 2023

Natural history and comorbidities of generalised and partial lipodystrophy syndromes in Spain

in Clinical Diabetes

Antía Fernández-Pombo
Sofía Sánchez-Iglesias
Ana I. Castro-Pais
Maria José Ginzo-Villamayor
Silvia Cobelo-Gómez
Teresa Prado-Moraña
Everardo Josué Díaz-López
Felipe F. Casanueva
Lourdes Loidi
David Araújo-Vilar

Frontiers in Endocrinology

doi 10.3389/fendo.2023.1250203

5,091 views
15 citations

Original Research

Published on 26 Sep 2018

A Single Complex Agpat2 Allele in a Patient With Partial Lipodystrophy

in Lipid and Fatty Acid Research

Marjoleine F. Broekema
Maarten P. G. Massink
Joep De Ligt
Edwin C. A. Stigter
Houshang Monajemi
Jeroen De Ridder
Boudewijn M. T. Burgering
Gijs W. van Haaften
Eric Kalkhoven

Frontiers in Physiology

doi 10.3389/fphys.2018.01363

4,249 views
10 citations

Case Report

Published on 24 Jul 2024

Case report: First Chinese patient with family partial lipodystrophy type 6 due to novel compound heterozygous mutations in the LIPE gene

in Genetics of Common and Rare Diseases

Yimeng Zhou
Lin Zhang
Yang Ding
Yongzhen Zhai

Frontiers in Genetics

doi 10.3389/fgene.2024.1417613

2,789 views
2 citations

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

6,725 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

6,380 views
13 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

4,544 views
8 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

3,999 views
11 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

5,145 views
6 citations

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

5,439 views
5 citations

Original Research

Published on 26 Aug 2021

Identification of Potential Biomarkers for Psoriasis by DNA Methylation and Gene Expression Datasets

in Epigenomics and Epigenetics

Yong Liu
Shengnan Cui
Jiayi Sun
Xiaoning Yan
Dongran Han

Frontiers in Genetics

doi 10.3389/fgene.2021.722803

9,528 views
24 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

116 views

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

4,459 views
4 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

4,723 views

Case Report

Published on 20 Aug 2018

Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred

in Clinical Diabetes

Renan Magalhães Montenegro
Aline Dantas Costa-Riquetto
Virgínia Oliveira Fernandes
Ana Paula Dias Rangel Montenegro
Lucas Santos de Santana
Alexander Augusto de Lima Jorge
Lia Beatriz de Azevedo Souza Karbage
Lindenberg Barbosa Aguiar
Francisco Herlânio Costa Carvalho
Milena Gurgel Teles

Frontiers in Endocrinology

doi 10.3389/fendo.2018.00458

6,429 views
19 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

1,059 views
2 citations

Articles

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

Natural history and comorbidities of generalised and partial lipodystrophy syndromes in Spain

A Single Complex Agpat2 Allele in a Patient With Partial Lipodystrophy

Case report: First Chinese patient with family partial lipodystrophy type 6 due to novel compound heterozygous mutations in the LIPE gene

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

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

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

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

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

Identification of Potential Biomarkers for Psoriasis by DNA Methylation and Gene Expression Datasets

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

Gestational and neonatal outcomes of women with partial Dunnigan lipodystrophy

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

Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred

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