Momanyi, Alex; Mwangi, Paul; Ayumba, Barry; Lwegado, Ronald
(International Journal of Case Reports in Orthopaedics, 2021)
Apert syndrome is a rare genetic type I acrocephalosyndactyly disease characterized by craniofacial dysmorphism and syndactyly of the hands and feet. It assumes as an autosomal dominant inheritance ...