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Currarino syndrome (CS) phenotype, initially described as the triad of hemisacrum, anorectal malformation (ARM… Expand BACKGROUND AND PURPOSE: Percutaneous sacroplasty has recently gained attention as a potential treatment for sacral insufficiency… Expand Currarino syndrome (CS) is a peculiar form of caudal regression syndrome [also known as autosomal dominant sacral agenesis (OMIM… Expand BACKGROUND
Caudal regression syndrome (CRS) is a congenital heterogeneous constellation of caudal anomalies that include varying… Expand BackgroundLeiomyomatosis peritonealis disseminata (LPD) is a rare disease in which multiple smooth muscle or smooth muscle-like… Expand Purpose: Urinary control after definitive repair of a cloacal anomaly is difficult to achieve. The present report aims to… Expand BACKGROUND/PURPOSE
The Currarino syndrome (CS) is a peculiar form of caudal regression syndrome (CRS) characterized by the… Expand The autosomal dominant Currarino anomaly (CA) comprises a presacral mass, partial sacral agenesis, and anorectal defects. Chronic… Expand Sacral agenesis is a heterogeneous group of congenital anomalies in which most cases are sporadic but rare familial forms also… Expand Anorectal malformations (ARMs) are common congenital anomalies that account for 1:4 digestive malformations. ARM patients show… Expand