Results 31 to 40 of about 4,679 (179)

Case‐malformed signal detection and prioritisation using EUROmediCAT data for pharmacovigilance in pregnancy

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Aim Many women take medications during pregnancy. However, the risk to the fetus from most medications is uncertain. Congenital anomalies are one of the leading causes of infant death and contribute to long‐term disability. Signal detection methods can be used to systematically identify possible medication–anomaly associations that require further ...
Hannah Johnson   +22 more
wiley   +1 more source

Congenital short bowel syndrome: Clinical aspects by systematic review

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund   +2 more
wiley   +1 more source

Necrotizing Enterocolitis Following Gastroschisis Repair: An Update

open access: yesGraduate Medical Education Research Journal, 2019
Introduction: Necrotizing enterocolitis (NEC) is a known complication of gastroschisis with an incidence above the expected rate in the neonatal population.
Rachel K. Schlueter   +3 more
doaj   +1 more source

Twin Pregnancy with Gastroschisis in Both Twins

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2007
Objective: Gastroschisis is a congenital malformation characterized by an abdominal wall defect located laterally to a normal umbilicus. The cause of gastroschisis is unknown, but most authors consider it exogenous. We describe the case of a woman with a
Hui-Fen Kao   +3 more
doaj   +1 more source

Therapeutic Hypothermia Treatment for an Infant with Hypoxic-Ischemic Encephalopathy and Gastroschisis: A Case Report

open access: yesAmerican Journal of Perinatology Reports, 2023
Gastroschisis is a congenital, typically isolated, full-thickness abdominal wall defect in which the abdominal contents, usually only the small intestine, remain outside the abdominal cavity.
Nicole Flores-Fenlon   +3 more
doaj   +1 more source

Early Outcome of Patient Born with Gastroschisis and Omphalocele

open access: yesمجلة كلية الطب, 2022
Background: Gastroschisis and omphalocele are the most common congenital defects of the anterior abdominal wall which need urgent and prompt intervention post-operative time outcomes of gastroschisis and omphalocele differ between different countries ...
Salar Berdawd, Abdulrahman O. Taha
doaj  

Gastroschisis annual incidence, mortality, and trends in extreme Southern Brazil

open access: yesJornal de Pediatria, 2022
Objective: To analyze gastroschisis annual incidence, mortality rates, and trends in the Brazilian state of Rio Grande do Sul from the year 2000 to the year 2017.
Paulo Acácio Egger   +6 more
doaj   +1 more source

The incidence of gastroschisis [PDF]

open access: yesBMJ, 2006
Gastroschisis is the evisceration of the fetal intestine through a defect in the paraumbilical anterior abdominal wall with herniation of gastrointestinal structures into the amniotic cavity. Babies born with this condition are more likely to be born prematurely and to have had poor fetal growth.
openaire   +2 more sources

Genetic sequencing of children with malrotation and midgut volvulus: A cross‐sectional study

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Intestinal malrotation with midgut volvulus can cause a particularly severe form of pediatric intestinal failure and is often a cause of ultra‐short bowel syndrome (SBS), with longer dependence on parenteral nutrition. While malrotation can be found in several genetic syndromes, most occurrences of this condition are not associated ...
Jonathan A. Salazar   +9 more
wiley   +1 more source

Rare left-sided gastroschisis with isolated omental herniation

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Gastroschisis is classically defined as a right-sided abdominal wall defect, resulting in the herniation of abdominal contents without a protective membrane.
Rachael Cannon   +2 more
doaj   +1 more source

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