Apert Syndrome (Acrocephalo Syndactyly): A Rare but Recognizable Human Malformation Syndrome

Abstract

BACKGROUND:Apert syndrome is a rare autosomal dominant Mendelian disorder characterized by a set of recognizable patterns of human malformations, having paediatric, plastic surgical, Ortholpaedic and Dental implications requiring early recognition & effective management strategies for good Cosmetic and functional out-come.