Intracardiac amorphous tumor presenting in a patient with homocystinuria; a case report with literature review

Homocystinuria is a rare genetic disease with autosomal recessive pattern. It is reported to be highest in Arabian descend and could cause thrombosis, but mainly peripherally. Cardiac amorphous tumor has been recognized in the past 20 years and it is also a very rare cause primary benign tumor of th...

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Detalles Bibliográficos
Autores principales: Hama-Karim, Diar S., Othman, Yad N., Majeed, Zryan Salar, Ali, Razhan K., Mohammed, Arian, Muhamad, Han Nihad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9870922/
https://www.ncbi.nlm.nih.gov/pubmed/36704364
http://dx.doi.org/10.1016/j.radcr.2022.12.040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9870922/
https://www.ncbi.nlm.nih.gov/pubmed/36704364
http://dx.doi.org/10.1016/j.radcr.2022.12.040

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