Linear IgA bullous disease (LABD) is a rare autoimmune subepidermal bullous disease characterized by linear deposits of IgA anti-basement membrane zone antibodies. The skin lesions are variable: papular, vesicular, bullous, erythematous, edematous, and erythema multiforme-like, mimicking bullous pemphigoid, dermatitis herpetiformis, toxic epidermal necrolysis, mucous membrane pemphigoid or in described case-Hailey-Hailey disease. We present a case of a 17-year-old female patient diagnosed with LABD associated with Hashimoto thyroiditis