ReviewPathologica2022
Congenital anomalies of the tubular gastrointestinal tract.
Review in Pathologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
18 citing papers in PubMed, 29 citations in OpenAlex.
- Jejunal Web Associated With Ileo-Ileal Intussusception in a 10-Month-Old Female Infant: A Rare Case Report.Clinical case reports · 2026Article
- Management of midgut volvulus in an incomplete common mesentery in a 17-year-old patient: a case report and literature review.International journal of surgery case reports · 2026Article
- Congenital intrinsic proximal jejunal obstruction caused by a mucosal web near the duodenojejunal junction in a neonate: a case report and literature review.Journal of surgical case reports · 2026Article
- Advancing enhanced recovery after surgery protocols for pediatric laparoscopic-assisted small intestinal malformation repair.BMC pediatrics · 2026Article
- Congenital Jejunal Web with Central Aperture in Children: Report of Two Cases of Delayed Diagnosis and Management.European journal of pediatric surgery reports · 2026Article
- Association Between Congenital Gastrointestinal Malformation Outcome and Largely Asymptomatic SARS-CoV-2 Infection in Pediatric Patients-A Systematic Review.Journal of clinical medicine · 2025Review
- Global, regional, and national burden of digestive congenital anomalies from 1990-2021.Pediatric research · 2025Article
- Abnormal anatomical landmarks: the guide points of laparoscopic Ladd's surgery for neonatal congenital intestinal malrotation.Surgical endoscopy · 2025Article
- Transverse colonic atresia with rectal atresia in a neonate - A rare case of double-site intestinal atresia.International journal of surgery case reports · 2025Article
- Unravelling a pediatric enigma: coexisting retroesophageal right subclavian artery and congenital colonic stenosis masquerading as cow's milk protein allergy and ileus in a neonate.BMC pediatrics · 2025Article
- Tissue-engineered tracheal implants: Advancements, challenges, and clinical considerations.Bioengineering & translational medicine · 2024Review
- Successful Endoscopic Treatment of a Pancreatic Pseudocyst in a Patient with Situs Inversus Totalis and Upper GI Duplication.The American journal of case reports · 2024Article
- Review
- An unusual case of colonic duplication cyst in an adult with dysplasia.Journal of surgical case reports · 2023Article
- Case report: Ileocecal preservation for multiple small intestinal duplications.Frontiers in pediatrics · 2023Article
- Congenital anomalies of the gastrointestinal tract: the liver, extrahepatic biliary tree and pancreas.Pathologica · 2022Review
- Congenital anomalies of the upper digestive tract: a review of esophageal and gastric embryology and malformations.Radiologia brasileiraReview
- Systematic Review of the Prevalence of Gastrointestinal Congenital Anomalies: A Global and Regional Review Protocol.Sage open pediatricsReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Congenital anomalies of the tubular gastrointestinal tract are an important cause of morbidity not only in infants, but also in children and adults. The gastrointestinal (GI) tract, composed of all three primitive germ layers, develops early during embryogenesis. Two major steps in its development are the formation of the gut tube (giving rise to the foregut, the midgut and the hindgut), and the formation of individual organs with specialized cell types. Formation of an intact and functioning GI tract is under strict control from various molecular pathways. Disruption of any of these crucial mechanisms involved in the cell-fate decision along the dorsoventral, anteroposterior, left-right and radial axes, can lead to numerous congenital anomalies, most of which occur and present in infancy. However, they may run undetected during childhood. Therapy is surgical, which in some cases must be performed urgently, and prognosis depends on early diagnosis and suitable treatment. A precise pathologic macroscopic or microscopic diagnosis is important, not only for the immediate treatment and management of affected individuals, but also for future counselling of the affected individual and their family. This is even more true in cases of multiple anomalies or syndromic patterns. We discuss some of the more frequent or clinically important congenital anomalies of the tubular GI, including atresia's, duplications, intestinal malrotation, Meckel's diverticulum and Hirschsprung's Disease.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.