Results 61 to 70 of about 1,537 (194)
Uncovering the Genetic Landscape of Spinal Dysraphism: A Retrospective Analysis of 150 Fetal Cases
ABSTRACT Objective Spinal dysraphism (SD) results from incomplete neural tube closure and encompasses a heterogeneous group of congenital anomalies with genetic and environmental etiologies. Although genetic contributions are recognized, causative variants remain insufficiently defined, and the clinical implications of extended genetic testing on ...
I. Bedei +9 more
wiley +1 more source
ABSTRACT Objective To describe prenatal imaging findings and postnatal outcomes in fetuses diagnosed with saccular forms of closed spinal dysraphism (CSD). Methods This retrospective single‐centre study included fetuses diagnosed with non‐genetic, non‐syndromic CSD between January 2018 and June 2023.
Yada Kunpalin +8 more
wiley +1 more source
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.70022 Abstract Aim To examine the accuracy of prenatal counselling at a multidisciplinary fetal neurology clinic (FNC) that led to termination of pregnancy (TOP), to improve the quality of future consultations. Method This retrospective diagnostic cohort study compared the imaging
Avi Shariv +12 more
wiley +1 more source
Prenatal Diagnosis of Congenital Dermal Sinus [PDF]
Background Congenital dermal sinus (CDS) is an uncommon form of spinal dysraphism. Although postdelivery identification in the neonate is aided by several associated physical examination findings, establishing this diagnosis prenatally has proven to be ...
Gonik, Bernard +4 more
core +6 more sources
Neonatal Arnold–Chiari II Malformation: An Imaging‐Focused Case Report
ABSTRACT Arnold‐Chiari Malformation Type II (CM‐II) is a serious congenital hindbrain disorder marked by the displacement of the cerebellum and brainstem downwards through the foramen magnum. CM‐II is frequently linked with myelomeningocele and hydrocephalus.
Mohammad Alashqar +8 more
wiley +1 more source
Pattern of Presentation of Spinal Dysraphism [PDF]
Objective: To assess the pattern of presentation of spinal dysraphism and compare with already available data on the subject. Design: Prospective study. Material and Method: This prospective study was done in the department of
MUBASHER AHMED, SAJID HUSSAIN MUGHAL
core +1 more source
ABSTRACT Aims To investigate factors affecting the quality of life of parents of children with spina bifida and examine how family resilience mediates between parental depression and quality of life. Design Cross–sectional study. Methods Secondary data analysis was performed using first‐year data from a five‐year spina bifida cohort project (2022–2026)
Kyua Kim +5 more
wiley +1 more source
Introduction of a urodynamic score to detect pre- and postoperative neurological deficits in children with a primary tethered cord [PDF]
Object: An increasing number of asymptomatic children are diagnosed with occult spinal dysraphism, raising the question of their optimal management. Urodynamic study (UDS) is the most reliable method of detecting neuro-urological abnormalities in these ...
Forcada-Guex, Margarita +5 more
core
Congenital anomalies of the vertebrae in dogs [PDF]
In this review article, a overview is given of the congenital pathologies of vertebrae in the dog. These pathologies are common in dogs and can be divided in two major groups: neural tube defects or spinal dysraphism, such as spina bifida with or without
De Rycke, Lieve, Saunders, Jimmy
core +1 more source
Validation of QUALAS-T, a health-related quality of life instrument for teenagers with spina bifida [PDF]
Introduction We aimed to develop and validate a self-reported QUAlity of Life Assessment in Spina bifida for Teenagers (QUALAS-T). Material and methods We drafted a 46-question pilot instrument using a patient-centered comprehensive item generation ...
Cain, Mark P. +9 more
core +1 more source

