Disease: Sacrococcygeal dysgenesis association
- Caudal Agenesis : Understanding the Base of the Wide Clinical Spectrum
- Caudal Regression Syndrome - a rare congenital disorder: A case report
- Early prenatal diagnosis of an atypical phenotype of sacral spina bifida
- Exome sequencing identifies variants in infants with sacral agenesis
- Experience with human tail and its outcome
- Functional fecal and urinary outcomes after sacrococcygeal mass resection in pediatric patients
- Multimodality Imaging Evaluation of Fetal Spine Anomalies with Postnatal Correlation
- Occurrence of rod fracture and salvage methods after primary surgery of the congenital lumbosacral deformity associated with sacral agenesis
- Posterior urethral valves masquerading as neuropathic bladder following sacrococcygeal teratoma resection
- Presacral neuroendocrine tumors associated with the Currarino syndrome
- Retained Medullary Cord Associated with Terminal Myelocystocele and Intramedullary Arachnoid Cyst
- Role of urodynamics in male patients of high-anorectal malformations: a prospective study
- Sacrococcygeal dysgenesis association
- Superficial burn from application of v+pad to obtain hemostasis in an infant
- Supernumerary Kidneys Associated with Disorders of Sexual Development and Cloacal Anomaly: A Case Report
- The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene
- The first case of mosaic MNX1 mutation in an adult female with features of Currarino syndrome