Results 41 to 50 of about 5,214 (161)

Congenital Hernia of the Umbilical Cord: A Retrospective Case Study

open access: yesActa Medica Philippina, 2023
Congenital hernia of the umbilical cord (CHUC) is the rarest type of anterior abdominal wall defect, in which an intact umbilical ring is always present and viscera pass through the base of normal-looking umbilicus.This study was conducted to document the intraoperative findings and postoperative outcomes of patients with congenital hernia of the ...
Gupta, Umesh Kumar   +4 more
openaire   +2 more sources

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain‐expressed sodium channelopathies

open access: yesEpilepsia, Volume 67, Issue 7, Page 3629-3643, July 2026.
Abstract Objective Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis (NDEEMA) represents the most severe end of the gain‐of‐function (GOF) SCN1A disorder spectrum. Sporadic cases of congenital arthrogryposis have also been reported in individuals with SCN2A‐, SCN3A‐, and SCN8A‐related developmental and ...
Sopio Gverdtsiteli   +43 more
wiley   +1 more source

Incarcerated umbilical cord hernia: a case report

open access: yesJournal 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   +3 more
doaj   +1 more source

Intact cord resuscitation in newborns with congenital diaphragmatic hernia: insights from a lamb model

open access: yesFrontiers in Pediatrics, 2023
IntroductionCongenital diaphragmatic hernia (CDH) is a rare condition characterized by pulmonary hypoplasia, vascular dystrophy, and pulmonary hypertension at birth.
Baptiste Teillet   +23 more
doaj   +1 more source

MRI in Sheep Model for Myelomeningocele Repair Using a Novel Polymer and Other Dural Patches

open access: yesPrenatal Diagnosis, Volume 46, Issue 8, Page 1267-1277, July 2026.
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

Neonatal umbilical hernia: A simple noninvasive technique

open access: yesGlobal Pediatrics
Background: A congenital umbilical hernia is a common anomaly seen at birth or during infancy, as a small or large umbilical bulge or swelling due to herniation of the bowel or omentum, mostly requiring medical attention.
Jayalaxmi Shripati Aihole
doaj   +1 more source

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

open access: yesМедицинский 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   +5 more
doaj   +1 more source

Pregnancy Outcomes and Postnatal Health From Transferred Mosaic Embryos Following Preimplantation Genetic Testing for Aneuploidy

open access: yesiNew Medicine, Volume 2, Issue 2, June 2026.
This illustration synthesizes the methods and conclusion of this study, demonstrating that the transfer of mosaic embryos following reimplantation genetic testing for aneuploidy does not increase the risk to postnatal health. ABSTRACT Next‐generation sequencing (NGS) has increased the detection of mosaic embryos during preimplantation genetic testing ...
Lili Chen   +10 more
wiley   +1 more source

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

open access: yesJournal 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

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