Postnatal Diagnosis of Sacral Agenesis with Cerebral Atrophy: A Case Report

Authors: Liadi N1, Kayode Adedeji B*, Ahmed H and El Wadiah Z

DOI: 10.23880/jqhe-16000110

Volume 2, Issue 1

Abstract

Background: Caudal regression syndrome (CRS), also called sacral agenesis is a rare disorder with a spectrum of congenital malformations ranging from simple anal atresia to absence of sacral, lumbar and possibly lower thoracic vertebra. It has an overall incidence of 1 in 60,000 live births. Case Report: We present a postnatal diagnosed case of CRS, delivered at 36 weeks gestation to a multigravida with poorly controlled gestational diabetes. We highlight the associated findings, which include arthrogryposis, cerebebral atrophy, urogenital and cardiac lesions. Conclusion: Sacral agenesis is an uncommon entity; the management is quite challenging, requiring multi-disciplinary intervention. The outcome depends on the spectrum and severity of abnormalities.

Keywords: Sacral Agenesis; Postnatal; Diagnosis

View PDF