Limited Wegener’s granulomatosis is characterized by the absence of kidney disease and systemic vasculitis evidence, with a c-ANCA sensitivity of 65-70% [14]. Clinical presentation varies from asymptomatic to cough, dyspnea, hemoptysis, pleuritic chest pain, malaise, weight loss, and fever [15,16]. The gene discussed is PRTN3; the disease is granulomatosis with polyangiitis.