DOI: 10.36347/gamj.2024.v05i02.002

Pages: 27-30

Bart’syndrome (BS) is a rare genetic disorder affecting newborns which associate congenital skin aplasia (CCA) with all types of epidermolysis bullosa. A girl was admitted immediately after birth for an ulcerative lesion located on the medial part of the left knee, leg and foot, associated with a foot deformity. We performed a simple of the secretion (no germ was founded), and a biopsy that confirmed the diagnosis of epidermolysis bullosa. She benefits of a local care with honey. Orthopedic treatment of varus foot. After 2 ‘months of follow-up, she had a good recovery with a complete cutaneous regeneration. Genetic counseling was also recommended to the patient's parents but they refused to do so.