03-23-2014, 02:23 PM
The correct answer is B. This patient has dysplastic nevus syndrome, which is an autosomal dominant condition related in many affected families to the CMM1 gene on chromosome 1.
Associate the other answers with the following diseases: Birbeck granules, histiocytosis X; desmoglein 3, pemphigus; Leser-Trélat sign, seborrheic keratoses; Munro microabscesses, psoriasis.
Associate the other answers with the following diseases: Birbeck granules, histiocytosis X; desmoglein 3, pemphigus; Leser-Trélat sign, seborrheic keratoses; Munro microabscesses, psoriasis.