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

Deepak Sharma¹, Sachin Lamba², Anshul Maheshwari², Sweta Shastri³
¹Pt B.d. Sharma, Pgims, Rohtak, Haryana, India.
²S.m.s Medical College, Jaipur, Rajasthan, India.
³Nkp Salve Medical College, Nagpur, Maharashtra, India.

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.

Keywords: Aplasia cutis congenita, Bart’s syndrome, epidermolysis bullosa, neonate, type VII collagen (COL7A1)

Deepak Sharma, Sachin Lamba, Anshul Maheshwari, Sweta Shastri. A Neonate with Aplasia Cutis Congenita Type VI with Junctional Epidermolysis Bullosa: A Very Rare Condition. Med J Islamic World Acad Sci. 2016; 24(3): 96-98

Sorumlu Yazar: Deepak Sharma, India

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