Introduction:-
Takayasu arteritis (TA), which was first described in 1908, is now acknowledged as an inflammatory disease of unknown origin that primarily affects the aorta and its main branches, pulmonary arteries, and coronary arteries in young females 1. The disease is characterized by inflammatory infiltrates involving all layers of the arteries, including acute exudative inflammation and chronic granulomatous inflammation primarily located in the media and adventitia along with hyperplasia and neovascularization of the intimal layer2. The wide range of clinical presentations associated with Takayasu arteritis makes its diagnosis challenging. This case study aims to illustrate the clinical features, diagnostic assessment, and treatment approach for Takayasu arteritis in a 22-year-old female presenting with neurological symptoms.