Von Hippel–Lindau syndrome with a rare complication of dilated cardiomyopathy: a case report

BACKGROUND: Von Hippel–Lindau (VHL) syndrome is an autosomal dominant hereditary disease affecting multiple organs, with pheochromocytoma in 26% of cases. However, VHL syndrome with congestive heart failure and dilated cardiomyopathy as the primary clinical manifestations has been rarely reported. C...

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Detalles Bibliográficos
Autores principales: Yu, Ming, Du, Beibei, Yao, Shuai, Ma, Jianghong, Yang, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673439/
https://www.ncbi.nlm.nih.gov/pubmed/36401171
http://dx.doi.org/10.1186/s12872-022-02913-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673439/
https://www.ncbi.nlm.nih.gov/pubmed/36401171
http://dx.doi.org/10.1186/s12872-022-02913-1

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