Step 1: Analyse the clinical presentation.
A 12-year-old boy with weak/absent pulses in upper limbs, low blood pressure (90/60 mmHg), and retinal haemorrhages. This combination points to large-vessel vasculitis affecting the aorta and its branches.
Step 2: Recall Takayasu arteritis.
Takayasu arteritis (pulseless disease / Martorell syndrome / occlusive thromboaortopathy) is a chronic granulomatous vasculitis predominantly affecting the aorta and its primary branches. It most commonly affects young females and adolescents. Features include: weak or absent pulses (especially upper limb), blood pressure discrepancy between limbs, bruits over subclavian/carotid arteries, claudication, vision problems (retinal haemorrhages, cotton-wool spots due to ocular ischaemia), and hypertension.
Step 3: Eliminate distractors.
PAN: affects medium-sized vessels, spares the lungs, causes renal and mesenteric involvement, not typically causing upper limb pulse loss.
Microscopic polyangiitis: small vessel ANCA-associated vasculitis causing glomerulonephritis and pulmonary haemorrhage.
HSP: IgA-mediated small vessel vasculitis causing palpable purpura on buttocks/legs, arthritis, abdominal pain, haematuria -- no pulse deficits.
Step 4: Confirm.
Absent upper limb pulses + low BP + retinal haemorrhages in a young patient = Takayasu arteritis.