ABSTRACT
La secuencia de displasia caudal (SDC), denominada también síndrome de regresión caudal y síndrome de agenesia sacra, es una malformación congénita poco frecuente, que incluye principalmente agenesia con extensión variable de cuerpos vertebrales distales lumbosacrococcígeos y/o sacrococcígeos. En este trabajo se presentan criterios diagnósticos por imagen, clasificación y estudio de un caso clínico.
Caudal dysplasia sequence (CDS), also called caudal regression syndrome and syndrome of sacral agenesis is a rare congenital malformation, which includes agenesis with variable extension of lumbo-sacral-coccygeal distal and sacrococcygeal vertebral bodies. In this article we review diagnostic criteria, classification and report a clinical case.
ABSTRACT
Sacral agenesis is a rare condition. This syndrome was first described by Hohl in 1852 and is usually associated with other anomalies such as vertebral deformities, deformed hypoplastic legs, urologic and gastrointestinal problems. We have experienced two cases of this deformity; one with partial sacral agenesis, and the other with partial lumbar agenesis and complete absence of sacrum.