Fraser Syndrome: A Rare Case Report

Abstract

Fraser syndrome is a rare, autosomal recessive condition. It is characterized by cryptophthalmos, syndactyly, craniofacial dysmorphism, laryngeal and genitourinary malformations, and musculoskeletal anomalies. We report a case of a neonate who presented with multiple congenital abnormalities and clinical features suggestive of Fraser syndrome.

Keywords

• Cryptophthalmos
• Fraser Syndrome
• Neonate
• Syndactyly