Results 41 to 50 of about 31,090 (171)

Emergency treatment of a ruptured huge omphalocele by simple suture of its membrane [PDF]

open access: yesAnnals of Surgical Innovation and Research, 2012
La ruptura de un onfalocele enorme es una emergencia que amenaza la vida del recién nacido. Constituye una preocupación terapéutica en ausencia de prótesis, especialmente en los países en desarrollo. Estamos informando aquí el caso de un bebé recién nacido que manejamos en emergencia con éxito gracias a un tratamiento simple.
Akakpo-Numado, Gamedzi Komlatse   +6 more
openaire   +2 more sources

Exploring hemodynamic alterations in gastroschisis: insights into fetal growth restriction using prenatal MRI

open access: yesUltrasound in Obstetrics &Gynecology, Volume 67, Issue 6, Page 795-805, June 2026.
Abstract Objective Despite the high incidence of fetal growth restriction (FGR) in gastroschisis (GS) associated with placental fetal vascular malperfusion (FVM), the underlying mechanism remains unclear. We aimed to investigate whether umbilical vein (UV) stenosis at the abdominal wall defect impairs fetoplacental circulation, leading to FGR.
H. Shi   +8 more
wiley   +1 more source

Diagnosis, management and prevention of umbilical infections in bovine youngstock

open access: yesIn Practice, Volume 48, Issue 3, Page 119-126, April 2026.
Background: Umbilical infections in calves demonstrate varied presentations, ranging from subclinical to localised swellings to more severe, disseminated infections, with or without associated umbilical hernias. Hygiene is a key modifiable risk factor – good management practices are central to prevention.
George Lindley   +3 more
wiley   +1 more source

Prenatal Diagnosis to Postnatal Outcomes of Saccular Forms of Closed Spina Dysraphism: A Single Center Retrospective Study

open access: yesPrenatal Diagnosis, Volume 46, Issue 2, Page 219-228, February 2026.
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

Onfalocele: análise de 33 casos. [PDF]

open access: yes, 2001
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Arisa, Alessandro Mendes
core  

Separation of omphalopagus conjoined twins with ruptured omphalocele, complex biliary sharing and a choledochal cyst

open access: yesJournal of Pediatric Surgery Case Reports, 2019
Separating conjoined twins requires a multidisciplinary team to manage all the phases of care. These phases include initial resuscitation, managing the often discordant physiology between each twin prior to separation, planning for and carrying out the ...
Daniel K. Robie   +2 more
doaj   +1 more source

The Impact of Chlamydia Treatment During Pregnancy on Birth Defects in New York State

open access: yesBirth Defects Research, Volume 118, Issue 1, January 2026.
ABSTRACT Background Chlamydia trachomatis (CT) diagnoses are highest among females of reproductive age. Yet, little is known about adverse infant outcomes associated with treatment for CT infections during pregnancy, including birth defects. Methods Using de‐identified matched data from the New York State (NYS) Sexually Transmitted Infection ...
Elizabeth M. Boos   +6 more
wiley   +1 more source

A case report on acrania with omphalocele [PDF]

open access: yes, 2023
Congenital/fetal malformations are structural, functional, and/or biochemical molecular defects present at birth. Prevalence of congenital fetal anomalies in developing countries are 2 to 3% of newborns and about 94% of severe birth defects. Acrania is a
B., Tejaswinibandaru, D., Rita
core   +1 more source

Contemporary Outcomes of Neonatal Exomphalos: A 12‐Year Single‐Centre Experience

open access: yesPediatrics International, Volume 68, Issue 1, January/December 2026.
ABSTRACT Aim Exomphalos is a congenital abdominal wall defect associated with significant neonatal morbidity and mortality. Contemporary UK outcome data remain sparse. This study describes outcomes, anomalies, and management strategies for live‐born infants with exomphalos over a 12‐year period at a UK tertiary neonatal surgical centre.
Agana Gnanakuruparan   +2 more
wiley   +1 more source

PPP1R12A Mutation Presenting With Congenital Jejunal Atresia and Short Stature: A Pediatric Endocrinology Case Report

open access: yesCase Reports in Pediatrics, Volume 2026, Issue 1, 2026.
We report an 11‐year‐old Hispanic male with a PPP1R12A gene de novo heterozygous likely pathogenic mutation, p. (Gln13Arg) (CAG>CGG), c.38 A > G in Exon 1 (NM_002480.2), detected on whole‐exome trio sequencing during his short‐stature evaluation.
Rosita Saul   +5 more
wiley   +1 more source

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