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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2023
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| Materias: | |
| 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 |