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Title: Bart syndrome associated with skeletal deformities: An uncommon case report. Author: Shahidi-Dadras M, Niknezhad N, Asadi-Kani Z, Zaresharifi S, Hamedani B, Abdollahimajd F. Journal: Dermatol Ther; 2019 Nov; 32(6):e13131. PubMed ID: 31631476. Abstract: Bart syndrome is a rare genetic disorder characterized by aplasia cutis congenita, epidermolysis bullosa (EB), and nail abnormalities. We reported an unusual case of Bart syndrome associated with skeletal abnormalities and bilateral clubfoot.[Abstract] [Full Text] [Related] [New Search]