Clinical Spectrum of LMNA-Associated Type 2 Familial Partial Lipodystrophy: A Systematic Review

Type 2 familial partial lipodystrophy (FPLD2) is a laminopathic lipodystrophy due to pathogenic variants in the LMNA gene. Its rarity implies that it is not well-known. The aim of this review was to explore the published data regarding the clinical characterisation of this syndrome in order to bette...

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Detalles Bibliográficos
Autores principales: Fernandez-Pombo, Antia, Diaz-Lopez, Everardo Josue, Castro, Ana I., Sanchez-Iglesias, Sofia, Cobelo-Gomez, Silvia, Prado-Moraña, Teresa, Araujo-Vilar, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000975/
https://www.ncbi.nlm.nih.gov/pubmed/36899861
http://dx.doi.org/10.3390/cells12050725

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000975/
https://www.ncbi.nlm.nih.gov/pubmed/36899861
http://dx.doi.org/10.3390/cells12050725

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