Currarino Syndrome in homozygous twins detected by following ultrasound during the fetal period.

The article focuses on Currarino triad or Syndrome is a rare dominant autosomal clinical condition that develops from the failure of the separation of the caudal cell mass from the hindgut endoderm dorso-ventrally. Topics include the neurulation of the cloaca results in occult dysraphic malformations anomalies, the variable combination of these malformations gives rise to a spectrum of clinical presentations, and the condition is characterized by the triad of sacral agenesis and presacral mass.