Bart syndrome associated with skeletal deformities: An uncommon case report.

Mohammad Shahidi-DadrasNasim NiknezhadZahra Asadi-KaniShirin ZaresharifiBehnaz Hamedani Fahimeh Abdollahimajd

Published in: Dermatologic therapy (2019)

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.

Keyphrases

case report
genome wide
gene expression