Congenital Disorders and Polyhydramnios with Suspected Edwards Syndrome

Abstract

The aim of this research is to identify and analyze congenital disorders and polyhydramnios with suspected Edwards syndrome. The method used in this study is a case report of a 43-year-old patient with a gravidity of G4P3A0H3 at 39-40 weeks of gestation. The results of this research indicate that congenital anomalies are inherent and defined as structural, functional, or metabolic abnormalities due to malformation of the contents. In 2010, congenital anomalies accounted for 10.5% of neonatal deaths. These anomalies are congenital in nature and are usually found independently, but multiple anomalies can be present together in a condition. Finding one anomaly can provide a favorable prognosis, but finding several anomalies can disrupt the baby's well-being. In the study, we report a neonate with congenital anomalies (anal atresia, micrognathia, bilateral cleft lip and palate, low-set ears, and rocker bottom foot). There is no history of illness, family and obstetric history, and no experiential disorders.