Takayasu arteritis is also known as pulseless disease and an autoimmune with unknown etiology which a rare type of chronic granulomatous vasculitis involving inflammation in the wall aorta its main branches such carotid, coronary, pulmonary renal arteries. The left subclavian artery most frequently involved vessel. can lead to narrowed walls that may tear, bulge ...

Takayasu’s Arteritis (TA), also known as pulseless disease, is a chronic large vessel vasculitis of unknown etiology that predominantly involves aorta and its major branches. Diagnosis TA remains challenging due to non-specific symptoms in childhood. We report 9 year old girl presenting with complaints fever short duration, associated severe pain abdomen. Clinical examination revealed decreased...

Background Takayasu disease is a non-specific inflammatory vasculitis of the large and medium caliber arteries occurring during 2nd or 3rd decade. Attachment before age 20 rare. Methods This retrospective descriptive study including patients with aged less than years out series 109 between 1984 2022 in department internal medicine vascular surgery at CHU INB SINA Rabat. Results We identified 11...