Caudal Regression Syndrome: A Case Report

Background: Lumbosacral agenesis or caudal regression syndrome (CRS) is a rare congenital malformation represented with symmetrical sacrococcygeal or lumbosacrococcygeal agenesis with a varied incidence between ۱ per ۲۵۰۰۰ live births to ۲.۵ per ۱۰۰۰۰۰ live births. Additionally, manifold abnormalities may be associated with CRS, including  spinal cord malformations, cardiac malformations, lipomyelomeningocele, orthopedic deformities, renal agenesis, neurogenic bladder, tethered-cord, sacral agenesis, and anorectal atresia.Case report: We report a case of a male neonate delivered to a ۲۸-year-old diabetic mother at ۳۸ weeks’ gestation diagnosed with CRS. In this case, lumbosacral agenesis, hip dislocation, and club foot deformities along with cardiac abnormalities, including small patent ductus arteriosus (PDA), atrial septal defect (ASD), hypertrophic cardiomyopathy (HCM) without left ventricular outlet obstruction were seen.Conclusion: Having the ۲۰۰-fold increased relative risk of developing CRS in infants of diabetic mothers in mind, this case report provides evidence that uncontrolled maternal diabetes might increase the risk of CRS  in infants.  

کلیدواژه ها:

Caudal regression syndrome ، Diabetes Mellitus ، Lumbosacral agenesis ، lumbosacral region ، Prenatal diagnosis