An Uncommon Association of Familial Partial Lipodystrophy, Dilated Cardiomyopathy, and Conduction System Disease

A 46-year-old African American woman presented with severe respiratory distress requiring intubation and was diagnosed with nonischemic cardiomyopathy. She had the typical phenotype of familial partial lipodystrophy 2 (FPLD2). Sequence analysis of LMNA gene showed a heterozygous missense mutation at...

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Detalles Bibliográficos
Autores principales: Panikkath, Ragesh, Panikkath, Deepa, Sanchez-Iglesias, S., Araujo-Vilar, D, Lado-Abeal, Joaquin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962337/
https://www.ncbi.nlm.nih.gov/pubmed/27504462
http://dx.doi.org/10.1177/2324709616658495

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962337/
https://www.ncbi.nlm.nih.gov/pubmed/27504462
http://dx.doi.org/10.1177/2324709616658495

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