Sacral Agenesis: Diagnosis, Treatment and Followup of Urological Complications

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Abstract
Sacral agenesis is an uncommon congenital anomaly that usually is accompanied by other orthopedic anomalies but often occurs singularly. Experiences in the treatment and long-term followup of 4 cases of pure sacral agenesis are reported. Early diagnosis and long-term careful follow are essential. The diagnosis was often overlooked and followup was poor. Studies must be undertaken to determine the type and degree of neurogenic vesicopathy in each child since that may vary from 1 patient to the next. The early and long-term use of intermittent catheterization is urged.