Danon Cardiomyopathy: Specific Imaging Signs

Danon disease (DD) is a rare, X-linked genetic disorder caused by LAMP2 deficiency. Clinical phenotype involves early cardiomyopathy development along with pre-excitation, skeletal myopathy, retinopathy, and cognitive impairment. We highlight how a noninvasive diagnostic approach based on clinical a...

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Detalles Bibliográficos
Autores principales: Miliou, Antigoni, Antonopoulos, Alexios S., Kouris, Nikos, Lazaros, George, Tsioufis, Konstantinos, Vlachopoulos, Charalambos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700059/
https://www.ncbi.nlm.nih.gov/pubmed/36444189
http://dx.doi.org/10.1016/j.jaccas.2022.08.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700059/
https://www.ncbi.nlm.nih.gov/pubmed/36444189
http://dx.doi.org/10.1016/j.jaccas.2022.08.007

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