Results 51 to 60 of about 9,146 (212)

Improving the Patient Experience in Pediatric Cystometrography: A Prospective Observational Study

Neurourology and Urodynamics, Volume 45, Issue 7, Page 1304-1312, September 2026.
ABSTRACT Introduction Cystometrography, despite its invasive nature, is a crucial investigation for understanding and managing the bladder in children with neurogenic, non‐neurogenic and congenital bladder conditions. Results are influenced by child behaviors and artefacts, but results can be critical in developing patient‐specific management plans ...
Assia Comella, Amy Bodley, Hayley Nugara, Edwina Mcdonald, Neil Price, Elizabeth Dally, Chris Kimber, Kiarash Taghavi   +7 more
wiley   +1 more source

Identification of potential key ferroptosis- and autophagy-related genes in myelomeningocele through bioinformatics analysis

Heliyon
Myelomeningocele is a common congenital anomaly associated with polygenic disorders worldwide. However, the intricate molecular mechanisms underlying myelomeningocele remain elusive. To investigate whether ferroptosis and ferritinophagy contribute to the
Xiuwei Wang, Kaixin Wei, Min Wang, Li Zhang   +3 more
doaj   +1 more source

Long-term follow-up of keystone perforator island flap in reconstructed myelomeningocele defects

JPRAS Open, 2023
Myelomeningocele (a type of spina bifida) is the most common congenital condition that causes lifelong physical disability and requires multi-system surgical procedures. Therefore, it is paramount to reconstruct them using a stable and robust method that
Tetyana Kelly, James Leong
doaj   +1 more source

Rare combination of Chiari II malformation with hydrocephalus, myelomeningocele, intracranial hemorrhage and sepsis in an Afghan neonate: A case report

Global Pediatrics
Background: Chiari malformation type 2 (CM2) is a rare congenital anomaly that is frequently associated with spinal dysraphism in neonates. The simultaneous presentation of CM2 with hydrocephalus, myelomeningocele, intracranial hemorrhage (ICH), caput ...
Mansoor Aslamzai, Mohammad Sharif Sediqi, Lutfullah Ahmadi, Turyalai Hakimi, Wahid Sekandari, Esrar Ahmad Mansoori   +5 more
doaj   +1 more source

Layered Closure of Lumbosacral Myelomeningocele Defects with Bilateral Paraspinous Muscle and Composite Fasciocutaneous Flaps

Plastic and Reconstructive Surgery, Global Open, 2020
Summary:. Robust, reliable, and reproducible closure of lumbosacral myelomeningocele defects remains a challenge. In infants with lumbosacral myelomeningocele defects, multiple methods of soft tissue coverage have been described.
Kathleen A. Holoyda, MD, Erinn N. Kim, MD, Fatma B. Tuncer, MD, Dino Maglic, MD, Ray C. Hosein, MD, John R. Kestle, MD, Faizi A. Siddiqi, MD, Barbu R. Gociman, MD, PhD   +7 more
doaj   +1 more source

Non-Targeted Metabolic Profiling of Cerebellum in Spina Bifida Fetal Rats

Metabolites, 2023
Spina bifida, known more commonly as myelomeningocele, is a neural tube defect that results in herniation of the cerebellum through the foramen magnum into the central canal as part of the Chiari II malformation.
Evan Thielen, Marc Oria, Miki Watanabe-Chailland, Kristin Lampe, Lindsey Romick-Rosendale, Jose L. Peiro   +5 more
doaj   +1 more source

First Case Report of an Infant with Aplasia Cutis Congenita of Scalp and Myelomeningocele

Brazilian Neurosurgery, 2016
Aplasia cutis congenita of scalp (ACCS) is a rare developmental anomaly. It has presented in children who have many concomitant anomalies. Large, deep defects can complicate by repeat local and systemic sepsis and life-threatening hemorrhage.
Angelo Silva Neto, Glena Marcelino, Cesar Garcia, Isadora Dantas, Isafran Silva, Emerson Oliveira   +5 more
doaj   +1 more source

Genomic Contributors to Congenital Diaphragmatic Hernia: Results of Exome Sequencing in 560 Probands and Cross Reference of Findings in an Independent Cohort

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1821-1831, August 2026.
ABSTRACT There is a strong genetic contribution to the etiology of congenital diaphragmatic hernia (CDH). This study evaluated genetic testing results and diagnostic yield for fetuses and children with CDH. This was a retrospective cohort study of exome sequencing (ES) performed at GeneDx for fetuses and children ≤ 18 years of age with CDH compared ...
Justin Blair, Kevin Carratu, Natalie E. Rintoul, Holly L. Hedrick, William H. Peranteau, Catherine M. Avitabile, Kirsty McWalter, Paul Kruszka, Ian D. Krantz, K. Taylor Wild   +9 more
wiley   +1 more source

Unilateral Bipedicled Subcostal and Lumbar Arteries Perforator Flap for Reconstruction of Large Myelomeningocele Defects [PDF]

Egyptian Journal of Plastic and Reconstructive Surgery, 2018
Background: A plenty of options have been described forreconstruction of large myelomeningocele defects. We reportedour experience of using bipedicled subcostal and lumbararteries perforator flap.Material and Methods: During a period of 31 months ...
Mohamed El Wahsh, Mahfouz Shehata
doaj   +1 more source

Lethal Consequences in an Infant with Myelomeningocele Following an Inadvertent Treatment

Journal of Forensic Science and Medicine, 2016
Myelomeningocele (MMC) is a protrusion of spinal cord contents and meninges through a vertebral defect. Iatrogenic deaths of patients with MMC are rarely encountered in forensic practice. In our case, a 3-month-old female was born with a lumbosacral cyst,
Xuemei Wu, Libing Yun, Min Liu, Xufu Yi
doaj   +1 more source