A Case of Infiltrative Cardiomyopathy Secondary to Primary Hyperoxaluria Type 2 - Utilization of Multimodality Imaging

Primary hyperoxaluria is a rare genetic disorder characterized by oxalate crystal deposition, including in the heart. Hyperoxaluria-associated cardiomyopathy manifests as restrictive infiltrative cardiomyopathy. We present a case of a 52-year-old male with a past medical history of type 2 primary hy...

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Detalles Bibliográficos
Autores principales: Lee, Dae Hyun, Kasprowicz, Thomas, Morales, Alberto, Sotolongo, Ignacio, Fernandez, Joel, Korabathina, Ravi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Cardiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515910/
https://www.ncbi.nlm.nih.gov/pubmed/34660109
http://dx.doi.org/10.7759/cureus.17914

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515910/
https://www.ncbi.nlm.nih.gov/pubmed/34660109
http://dx.doi.org/10.7759/cureus.17914

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