• A CASE OF UNCONTROLLED MATERNAL DIABETES MELLITUS ASSOCIATED WITH FETAL SACRAL AGENESIS
• A review of adopted colorectal patients: a parent's perspective
• A Surgical Case of Currarino Syndrome with Syringomyelia
• Allowing Standing and Assisted Steps in a Patient With Renshaw Type IV Sacral Agenesis: A Case Report of a Novel Surgical Approach
• Analysis of the potential risk factors for defecation problems and their bowel management based on the long-term bowel function in patients with persistent cloaca: results of a nationwide survey in Japan
• Association of spinal cord abnormalities with vertebral anomalies: an embryological perspective
• Atypical caudal regression syndrome with lumbar agenesis, hypoplastic sacrum without sacroiliac joints in the eastern Democratic Republic of Congo: a case report
• Beyond the Tailbone: A Family's Journey Through Caudal Regression Syndrome-A Triple Sibship
• Bladder Reconstruction with Bowel: Robot-Assisted Laparoscopic Ileocystoplasty with Mitrofanoff Appendicovesicostomy in Pediatric Patients
• Case report: Sacral agenesis in two boxer dogs: clinical presentation, diagnostic investigations, and outcome
• Caudal Agenesis : Understanding the Base of the Wide Clinical Spectrum
• Caudal regression in fetus with de novo SMARCA2 pathogenic variant
• Caudal Regression Syndrome
• Caudal Regression Syndrome - a rare congenital disorder: A case report
• Caudal regression syndrome (Currarino syndrome) with chromosom mutation 9
• Caudal regression syndrome from radiology and clinical perspective: A case series and a proposed new integrated diagnostic algorithm
• Caudal regression syndrome in a fetus of a glucokinase-maturity-onset diabetes of the young pregnancy
• Caudal regression syndrome type 1 with minimally invasive computed tomography and magnetic resonance imaging autopsy: a case report
• Caudal Regression Syndrome-A Narrative Review: An Orthopedic Point of View
• Caudal regression syndrome: Postnatal radiological diagnosis with literature review of 83 cases
• Cephalopagus twins diagnosed at 7 weeks gestational age following IVF/ICSI
• Characterization of complete Currarino syndrome in pediatrics-a comparison between CT and MRI
• Clinical and Radiological Characterization of an Infant with Caudal Regression Syndrome Type III
• Clinical and radiological evaluation of caudal regression syndrome
• Clinically Relevant Morphometry of Sacral Hiatus and Morphology of Sacrum
• Congenital Anterior Dislocation of the Sacrococcygeal Bone in a Newborn
• Congenital Risk Factors for Chronic Kidney Disease in Patients With Persistent Cloaca: Results From a Nationwide Survey in Japan
• Conjoined twins presenting with foot deformities: insights to management and challenges
• Continuous ultrasound-guided sacral intervertebral block for postoperative analgesia in neonates
• Currarino syndrome in an adult woman
• Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report
• Currarino syndrome: a comprehensive genetic review of a rare congenital disorder
• Currarino triad: A case report of a 48-year-old patient with a neuroendocrine tumor
• Descriptive and risk factor analysis of nonsyndromic sacral agenesis: National Birth Defects Prevention Study, 1997-2011
• Diabetic Embryopathies
• Diagnostic Utility of Spinal Ultrasounds in Neonates
• Differences in rectoanal inhibitory reflex duration between patients with refractory functional constipationand myelomeningocele
• Different distal fixation anchors in lumbosacral spinal deformities associated with sacral agenesis: which one is better?
• DNA methylation, combined with RNA sequencing, provide novel insight into molecular classification of chordomas and their microenvironment
• Effect of megarectum on postoperative defecation of female patients with congenital rectovestibular fistula or rectoperineal fistula
• Elongated Conus Medullaris, Sacral Agenesis, and Scoliosis: A Case Report of a Patient with Trisomy 19q and Monosomy 7q
• Evaluation and Long-term Management of Neurogenic Bladder in Spinal Dysraphism
• Exome sequencing identifies variants in infants with sacral agenesis
• Expansion Thoracoplasty as a Life-Saving Procedure in an Adolescent With Severe Spinal Deformity and Sacral Agenesis
• Factors affecting clean intermittent catheterization compliance among children and adolescents with neurogenic bladder due to spina bifida and caudal regression syndrome
• Fetal Magnetic Resonance Imaging in Association With Antenatal Ultrasound in the Diagnosis of Caudal Dysgenesis: Report of Two Cases
• High uterosacral ligament suspension in radical hysterectomy: a step-by-step procedure to prevent pelvic organ prolapse
• Hybrid Renal Cortical Imaging with Single Photon Emission Computerized Tomography/Computed Tomography in a Pediatric Patient with Severe Caudal Regression Syndrome
• Isokinetic strength assessment of trunk muscle and its relationship with spinal-pelvic parameters in patients with degenerative spinal deformity
• Kidney transplantation using a colon pouch (Mainz pouch III): a case report
• Klippel Feil Syndrome: Clinical Phenotypes Associated With Surgical Treatment
• Laparoscopic-assisted anorectoplasty for anorectal malformation with rectobulbar fistula: A two-center comparative study with posterior sagittal anorectoplasty
• Long-term outcomes in sacral agenesis
• Managing Recurrent Teratoma in Currarino Syndrome
• Medulloblastoma in association with sacral agenesis; a case report
• Molecular landscape of congenital vertebral malformations: recent discoveries and future directions
• Multiple Hemivertebrae: The Natural History and Treatment of 50 Patients
• Neonatal caudal regression syndrome
• Occurrence of rod fracture and salvage methods after primary surgery of the congenital lumbosacral deformity associated with sacral agenesis
• Patterns of multiple congenital anomalies in the National Birth Defect Prevention Study: Challenges and insights
• Pierre Robin syndrome with caudal regression syndrome-a rare combination of congenital syndromes
• Postoperative complications and long-term outcomes in Currarino syndrome
• Pregnancy in a woman with sacral agenesis from prenatal counseling to delivery: A case report
• Prenatal diagnosis of caudal regression with heterotaxy syndrome: "A mermaid with a broken heart"
• Presacral neuroendocrine tumors associated with the Currarino syndrome
• Prevalence of lumbosacral transitional vertebra in patients with chronic low back pain: a descriptive cross-sectional study
• Prominent caudal shift of the lumbar plexus roots in spines with 18 thoracolumbar vertebrae
• Radiological and clinical aspect of Caudal regression syndrome associated with dorsal hemivertebra without maternal diabetes
• Re: Factors affecting clean intermittent catheterization compliance among children and adolescents with neurogenic bladder due to spina bifida and caudal regression syndrome
• Rectal Prolapse Following Repair of Anorectal Malformation: Incidence, Risk Factors, and Management
• Rectothecal fistula complicating anterior sacral meningocele repair
• Results of a defined surgical protocol for treating pediatric neurogenic bladder incontinence in a single institution
• Risk of birth defects by pregestational type 1 or type 2 diabetes: National Birth Defects Prevention Study, 1997-2011
• Risk of Stillbirth for Fetuses With Specific Birth Defects
• Role of urodynamics in male patients of high-anorectal malformations: a prospective study
• Sacral agenesis and fecal incontinence: how to increase the index of suspicion
• Sacral agenesis combined with spinopelvic dissociation: A case report and literature review
• Sacral agenesis without maternal diabetes: a case report
• Sacral Agenesis: A Neglected Deformity That Increases the Incidence of Postoperative Coronal Imbalance in Congenital Lumbosacral Deformities
• Sacral Agenesis: Late Presentation and the Psychological Impact of Delayed Diagnosis
• Sacral neuromodulation in congenital lumbo-sacral and traumatic spinal cord defects with neurogenic lower urinary tract symptoms: a single-center experience in children and adolescents
• Sacral Tarlov cysts: Neurophysiology abnormalities and correlation with pelvic sensory and visceral symptoms
• Sagittal kinematics and imbalance of the spine and whole body during walking in late-onset Pompe disease
• Specific birth defects in pregnancies of women with diabetes: National Birth Defects Prevention Study, 1997-2011
• Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome
• Spina bifida occulta with the persistent spinous process in living: A three-dimensionally reconstructed sacrum from computed tomographic imaging
• Spinal dysraphism in exstrophy: a single-center study of a 39-year prospective database
• Stricture rate in patients after the repair of anorectal malformation following a standardized dilation protocol
• Successful Management of Limbal Dermoid in Infancy and Childhood: A Case Series
• Successful sacral neuromodulation treatment of refractory faecal incontinence in a patient with spina bifida and partial sacral agenesis
• Surgical Correction of Spinopelvic Instability in Children With Caudal Regression Syndrome
• Surgical Surprise during Posterior Sagittal Anorectoplasy: A Rectal Duplication
• The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene
• The importance of dedicated colorectal team participation in the management of spina bifida and spinal cord injury patients
• The influence of lumbo-sacral transitional vertebrae in developmental dysplasia of the hip: a matched pair analysis
• The Role of MRI in Children With Congenital Limb Deficiencies With Associated Scoliosis
• The treatment of congenital recto-vestibular fistula and recto-perineal fistula and effect of the megarectum on defecation
• Transcutaneous electrical stimulation for gastrointestinal motility disorders
• Turbulent Cerebrospinal Fluid Flow in Enlarging Terminal Myelocystocele
• Ultrasonographic images of spina bifida before obstetric anesthesia: a case series