ABSTRACT

Trisomy 18 (Edwards syndrome), is a syndrome characterized by multiple congenital anomalies, occuring together with excess 18. chromosome. Intrauterine growth retardation, micrognathia, microcephaly, low-set ears, cardiac abnormalities, urinary tract abnormalities, gastrointestinal tract anomalies and limb anomalies are the findings which are commonly encountered in infants with Edwards Syndrome. Here we aimed to present a case of 2 months old infant with multiple congenital anomalies and diagnosed as Edwards Syndrome.