Publications by authors named "Tahseen Ali Al-Kinani"
Article Synopsis
- Timely recognition of atypical Takayasu arteritis (TA) is essential, as unusual symptoms can complicate diagnosis.
- A specific case involved a 42-year-old male with pericardial effusion, where a CT angiogram confirmed the diagnosis of large vessel vasculitis.
- Successful management with immunosuppressive therapy highlights the need for collaborative care among various medical specialists to improve patient outcomes in TA.
Background: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a disorder that involves replacement of the right ventricular myocardium with fibro-fatty tissue. Ventricular tachycardia is a main presenting feature. There are no known reports of this disease from the Arab countries in the Middle East.
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