Bowen-Conradi syndrome, also known as BCS, is a rare genetic disorder that affects infants and young children. Some synonyms for BCS include Craniofacial microsomia, Ectodermal dysplasia-syndactyly syndrome, Tricho-rhino-phalangeal syndrome, and Frontometaphyseal dysplasia. These syndromes are characterized by a wide range of symptoms such as craniofacial abnormalities, developmental delays, and skeletal abnormalities. BCS is caused by mutations in the EMG1 gene and is inherited in an autosomal recessive pattern. While there is currently no cure for BCS, early diagnosis and management can significantly improve the quality of life for affected individuals.