Caudal regression syndrome (CRS) is a congenital disorder which is seen vertebral anomalies in varying degrees from lower thoracic spineto the level of the coccyx. We present a case of CRS which is not intended operation for orthopedic deformities considering functionality. 2, 5 year-old girl referred to our clinic with complaints about walking disability, knee and foot deformities. Patient's m...

To cite: Puneeth KT, Goyal A, Jana M. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013201770 DESCRIPTION A 10-month-old female infant, born to a diabetic mother, presented with dribbling of urine since birth. Physical examination was unremarkable. Plain radiograph of lower spine showed partial sacral agenesis. MRI of the spine (figure 1) revealed sacrococcygea...

     Urethralduplication is a rare condition occurs as a congenital malformation either independently or in the setting of other congenital malformations such as caudal duplication syndrome. Its prevalence becomes even rarer if it manifests as two side-by-side tracts in coronal plan.Nonetheless, we introduce a unique presentation of complete coronal urethral duplication accompanied by astoundin...

The Currarino triad, also known as the “Currarino Syndrome”, is a rare complex of congenital caudal anomalies including three main features; a sacral bony deformity, anorectal malformations, and a presacral mass. We present an extremely uncommon case of Currarino syndrome in adulthood presenting with repeated episodes of meningitis. Magnetic resonance imaging of spine was suggestive of caudal r...