Apert syndrome- a case report
Apert syndrome is a rare congenital disorder which is a part of Acrocephalosyndactyly syndromes. It is characterized by craniosynostosis, symmetrical syndactyly of hands and feet. We present a case of Apert syndrome with clinical features of brachycephaly, proptosis, flat forehead, low set ears with syndactyly of hands and feet.
Published in 2012.