Results 31 to 40 of about 1,046 (132)
Syringomyelia in children with closed spinal dysraphism: long-term outcomes after surgical intervention [PDF]
OBJECTIVEThe nature of the relationship between spinal cord syrinx and tethered cord is not well known. It is unclear if surgical cord untethering results in resolution or improvement of an associated syrinx. The objective of this study was to report the response of spinal cord syrinx to surgical cord untethering.METHODSThe authors retrospectively ...
Amy K, Bruzek +5 more
openaire +2 more sources
ABSTRACT Objectives To describe, characterize and determine the frequency of interhemispheric fissure (IHF) distortion on ultrasound in fetuses with open spina bifida (OSB), evaluate its association with other intracranial findings and biometric parameters and assess its evolution after prenatal closure of the spinal defect.
L. S. Carmant +7 more
wiley +1 more source
ABSTRACT Objectives To quantify the discrepancy between anatomical and motor levels in foetuses with open spinal dysraphism and identify prenatal factors associated with this difference. We also examined associations between anatomical level and ultrasound findings. Design Retrospective observational study.
Silvia Arévalo +8 more
wiley +1 more source
ABSTRACT A 7‐month‐old female presented with a congenital sacrococcygeal mass. While SCT and MMC are common, MRI ruled them out, leading to simple excision. Histopathology revealed a rare subcutaneous sacrococcygeal lipoma. This case emphasizes the use of advanced imaging to differentiate benign soft‐tissue lesions from spinal or neoplastic pathologies
Rajab Msemo +9 more
wiley +1 more source
ABSTRACT Currarino Syndrome (CS) should be suspected in infants presenting with persistent constipation and sacral anomalies. Early diagnosis using appropriate imaging and multidisciplinary surgical management is essential to prevent serious complications such as bowel obstruction, infection, and neurological impairment.
Ferdinand Medard Shilikale +4 more
wiley +1 more source
ABSTRACT The simultaneous occurrence of Arnold–Chiari Malformation Type II (ACM II), syringomyelia, and an acquired tracheoesophageal fistula (TEF) in a young adult is exceptionally rare and represents a major diagnostic challenge. Arnold–Chiari Malformation II is characterized by the herniation of cerebellar structures through the foramen magnum.
Zahabia Adnan +6 more
wiley +1 more source
MRI in Sheep Model for Myelomeningocele Repair Using a Novel Polymer and Other Dural Patches
ABSTRACT Objective To compare postnatal MRI outcomes after prenatal myelomeningocele repair using three different dural substitutes. Method 32 sheep fetuses were included, with 34.3%(11/32) serving as healthy controls and the remaining undergoing prenatal spinal lumbar defect creation to recreate a myelomeningocele in the fetus.
Usha D. Nagaraj +5 more
wiley +1 more source
ABSTRACT Aims To explore the boundary of clinical use of sacral nerve stimulation (SNS) in neurogenic lower urinary tract dysfunction (NLUTD), identifying barriers to approval and early‐impact research questions. Methods This review is derived from a proposal discussion at the International Consultation on Incontinence‐Research Society in Bristol in ...
Marcus J. Drake +6 more
wiley +1 more source
ABSTRACT Rachipagus parasitic twinning is an exceptionally rare clinical entity resulting from an asymmetric monozygotic twinning process, characterized by a dorsally co‐joined partially formed twin. Co‐ existence of this condition with neural tube defect is uncommon, yet clinically significant.
Biruk Lealem +2 more
wiley +1 more source
Predictors of long‐term outcome in open spina bifida
Developmental Medicine &Child Neurology, Volume 68, Issue 9, Page 1178-1179, September 2026.
Alison Poulton, Pippa Oakeshott
wiley +1 more source

