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

PURPOSE: Familial partial lipodystrophy type 2 (FPLD2) patients generally develop a wide variety of severe metabolic complications. However, they are not usually affected by primary cardiomyopathy and conduction system disturbances, although a few cases of FPLD2 and cardiomyopathy have been reported...

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Detalles Bibliográficos
Autores principales: Cecchetti, Carolina, D’Apice, M. Rosaria, Morini, Elena, Novelli, Giuseppe, Pizzi, Carmine, Pagotto, Uberto, Gambineri, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092436/
https://www.ncbi.nlm.nih.gov/pubmed/33953703
http://dx.doi.org/10.3389/fendo.2021.675096

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092436/
https://www.ncbi.nlm.nih.gov/pubmed/33953703
http://dx.doi.org/10.3389/fendo.2021.675096

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