Results 31 to 40 of about 5,049 (159)

Novel approaches for drug development against chronic primary pain: A systematic review

British Journal of Pharmacology, EarlyView.
Abstract Chronic primary pain (CPP) persisting for more than 3 months, associated with significant emotional distress without any known underlying cause, is an unmet medical need. Traditional or adjuvant analgesics do not provide satisfactory pain relief for a great proportion of these patients.
Valéria Tékus, Éva Borbély, Andreas Goebel, Ralf Baron, Zsófia Hajna, Zsuzsanna Helyes   +5 more
wiley   +1 more source

Posttraumatic both loop ileal prolapse through patent vitello-intestinal duct in a neonate: A rare occurrence

Muller Journal of Medical Sciences and Research, 2016
Umbilical cord hernia (UCH) is consisting of 20% of all congenital abdominal wall defects. Vitello-intestinal duct (VID) is the communicating embryonic structure which disappears between the 5 th and 9 th weeks of intrauterine life.
Md Hadiuzzaman Zaman, Shibsankar Barman, Sumitra Kumar Biswas, Kalyani Saha Basu   +3 more
doaj   +1 more source

Female Patients With Mucopolysaccharidosis II (MPS II): Insights From the Hunter Outcome Survey

JIMD Reports, Volume 67, Issue 1, January 2026.
ABSTRACT Mucopolysaccharidosis II is a rare, X‐linked disease, with very few reports of affected female patients. Natural history data describe a predominantly male population, and appropriate disease characterization in female patients is lacking. This analysis explores the somatic disease burden and clinical progression of female patients with MPS II
Barbara K. Burton, Hernan Amartino, Roberto Giugliani, Christoph Kampmann, Julian Raiman, Maurizio Scarpa, Anna Tylki‐Szymańska, Jennifer Audi, Jaco Botha, Siddarth Jain, Joseph Muenzer   +10 more
wiley   +1 more source

Selected Abstracts of the 12th International Congress of UENPS; Krakow (Poland); September 2nd-4th, 2022

Journal of Pediatric and Neonatal Individualized Medicine, 2022
Selected Abstracts of the 12th International Congress of UENPS; Krakow (Poland); September 2nd-4th, 2022  The Congress has been organized by the Union of European Neonatal and Perinatal Societies (UENPS).    ABS 1.
--- Various Authors
doaj   +1 more source

Combining Detailed Fetal Anatomy Scanning in the NT Window Versus Early Second Trimester Scanning at 14–16 Weeks

Journal of Ultrasound in Medicine, Volume 45, Issue 1, Page 105-113, January 2026.
Objectives First‐trimester ultrasound has evolved to incorporate a detailed fetal anatomy scan (FAS) with nuchal translucency (NT) screening. Many institutions use a 2‐visit protocol: NT followed by detailed FAS at 14–16 weeks. We aimed to evaluate whether integrating detailed FAS into the NT window (12 + 5 to 13 + 6 weeks) is non‐inferior in ...
Tomer Shwartz, Sarah M. Cohen, Michal Lipschuetz, Hila Hochler, Yaron Zalel, Dan V. Valsky, Simcha Yagel   +6 more
wiley   +1 more source

Combined negative pressure wound therapy with irrigation and dwell time and artificial dermis prevents infection and promotes granulation formation in a ruptured giant omphalocele: a case report

BMC Pediatrics, 2022
Background Omphalocele is a congenital abdominal wall defect of the umbilical cord insertion site. A giant omphalocele, with a fascial defect > 5 cm in diameter and/or containing > 50% of the liver within the hernia sac, can be challenging for pediatric ...
Yoichi Nakagawa, Hiroo Uchida, Akinari Hinoki, Chiyoe Shirota, Wataru Sumida, Satoshi Makita, Hizuru Amano, Masamune Okamoto, Aitaro Takimoto, Seiya Ogata, Shunya Takada, Daiki Kato, Yousuke Gohda   +12 more
doaj   +1 more source

Exploration of the Pathogenic Mechanism of the Factor XIII A Subunit in a Patient With Congenital Factor XIII Deficiency

Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
This study identifies a novel Ser414Leu variant in the F13A1 gene associated with congenital FXIII deficiency, demonstrating its potential to destabilize the protein structure. ABSTRACT Background Congenital factor XIII (FXIII) deficiency is an extremely rare autosomal recessive blood clotting disorder with an incidence of approximately one in two ...
Min Wang, Nan Wei, Tianping Chen, Aoshuang Jiang, Yinghui Zhao, Chenglin Zhu, Lijuan Zhu, Lijun Qu, Hongjun Liu   +8 more
wiley   +1 more source

Incarcerated umbilical cord hernia: a case report

Journal of Pediatric Surgery Case Reports
Introduction: Congenital hernia of the umbilical cord (CHUC) is a rare developmental anomaly that results from the incomplete return of the midgut into the abdominal cavity during fetal development. It is often misdiagnosed as a small omphalocele and may
Mohammed Alra'e, Maaweya Jabareen, Wasef Alhroub, Radwan Abukarsh   +3 more
doaj   +1 more source

Can Prenatal Ultrasonographic Markers Predict Enteral Feeding Tolerance in Neonates With Fetal Omphalocele?

Prenatal Diagnosis, Volume 46, Issue 1, Page 21-29, January 2026.
ABSTRACT Objective This study aimed to identify prenatal ultrasonographic predictors of enteral feeding tolerance in neonates with omphaloceles. Method This retrospective cohort study included all live‐born neonates prenatally diagnosed with omphalocele at Emma Children's Hospital/Amsterdam UMC approximately 2004–2024.
Maaike Hogerwerf, Hanna Heinrich, Merit M. Tabbers, Ramon R. Gorter, Bart G. P. Koot, Jos W. R. Twisk, Eva Pajkrt, Joep P. M. Derikx   +7 more
wiley   +1 more source

OUTPATIENT MANAGEMENT OF A PATIENT WITH BECKWITHWIEDEMANN SYNDROME (CASE REPORT)

Медицинский совет, 2017
Beckwith - Wiedemann syndrome (ICD-10 code: Q 87.3) is a congenital disease characterized by macrosomia, macroglossia, hernia umbilical cord, overgrowth in the first few years of life, asymmetry of the body and a predisposition to embryonal tumor ...
E. A. Kashirina, A. A. Rubtsova, N. M. Yugai, O. B. Karabanova, O. V. Chernokozheva, S. G. Zagidullina   +5 more
doaj   +1 more source