Inflammatory myopathy in the context of an unusual overlapping laminopathy

Laminopathies are genetic disorders associated with alterations in nuclear envelope proteins, known as lamins. The LMNA gene encodes lamins A and C, and LMNA mutations have been linked to diseases involving fat (type 2 familial partial lipodystrophy [FPLD2]), muscle (type 2 Emery–Dreifuss muscular d...

Descripción completa

Detalles Bibliográficos
Autores principales: Guillín-Amarelle, Cristina, Sánchez-Iglesias, Sofía, Mera, Antonio, Pintos, Elena, Castro-Pais, Ana, Rodríguez-Cañete, Leticia, Pardo, Julio, Casanueva, Felipe F., Araújo-Vilar, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Endocrinologia e Metabologia 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118788/
https://www.ncbi.nlm.nih.gov/pubmed/29791652
http://dx.doi.org/10.20945/2359-3997000000048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118788/
https://www.ncbi.nlm.nih.gov/pubmed/29791652
http://dx.doi.org/10.20945/2359-3997000000048

Ejemplares similares