A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition

This study aimed to describe a case of aplasia cutis congenita with epidermolysis bullosa, as only a few reports of Bart’s syndrome exist in the medical literature. Aplasia cutis congenita (ACC) is a rare dermatological condition characterized by the absence of skin. It has no proven etiology and hence stills remains a mystery for the dermatologist of the modern world. The most common body part affected is the scalp. ACC with epidermolysis bullosa (Bart’s syndrome) is a very rare variant of aplasia cutis.