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

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

PurposeFamilial 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 i...

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Bibliographic Details
Main Authors: Carolina Cecchetti, M. Rosaria D’Apice, Elena Morini, Giuseppe Novelli, Carmine Pizzi, Uberto Pagotto, Alessandra Gambineri
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-04-01
Series:Frontiers in Endocrinology
Subjects:
lipodystrophy
rod domain
LMNA gene
cardiomyopathy
laminopathy
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2021.675096/full

Internet

https://www.frontiersin.org/articles/10.3389/fendo.2021.675096/full

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