A 19-year-old male with truncus arteriosus type I: a rare case report from Syria
This case report underscores the complexities in managing a 19-year-old male with Eisenmenger syndrome, emphasizing the need for a conservative approach and continual monitoring to enhance patient outcomes.
Authors
- Abdulrahman Ahmad Othman (ORCID: https://orcid.org/0009-0000-2760-5972)
- Intan Hakimah Ismail (ORCID: https://orcid.org/0000-0003-4614-0140)
- Mouhammed Sleiay (ORCID: https://orcid.org/0009-0003-8887-0739)
- Saleh Takkem
- Abdulrahim Hamad Alokla
- M-Jaber Kojak
- Obada Al Tawekji
- Ahmad Alhamid (ORCID: https://orcid.org/0009-0002-6478-314X)
- Abdullah Alomar
- Abdulkader Bitar
- Molham Homsi
Institutions
- Syrian Private University (SY)
- Al-Hawash Private University
- Damascus University (SY)
- Saarland University (DE)
Publication Details
- Journal
- Annals of Medicine and Surgery
- Published
- 2025-03-07
- DOI
- https://doi.org/10.1097/ms9.0000000000003145
- Citations
- 1
- Primary Topic
- Congenital Heart Disease Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.35