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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1945 2
1947 4
1948 5
1949 7
1950 3
1951 5
1952 5
1953 3
1954 2
1955 5
1956 6
1957 9
1958 3
1959 5
1960 3
1961 2
1962 7
1963 17
1964 14
1965 10
1966 12
1967 9
1968 13
1969 8
1970 9
1971 13
1972 7
1973 6
1974 10
1975 14
1976 16
1977 14
1978 20
1979 32
1980 20
1981 37
1982 38
1983 27
1984 29
1985 28
1986 32
1987 39
1988 32
1989 41
1990 42
1991 39
1992 35
1993 35
1994 27
1995 31
1996 47
1997 34
1998 44
1999 36
2000 42
2001 43
2002 38
2003 34
2004 38
2005 41
2006 53
2007 67
2008 76
2009 64
2010 68
2011 56
2012 64
2013 61
2014 85
2015 73
2016 66
2017 62
2018 64
2019 76
2020 84
2021 88
2022 83
2023 99
2024 80
2025 106
2026 39

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103 results

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Page 1
Omphalocele.
Zahouani T, Mendez MD. Zahouani T, et al. 2023 May 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 May 23. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 30085552 Free Books & Documents.
Omphalocele is a rare congenital abdominal wall defect with a reported prevalence of 3.38 per 10,000 pregnancies. ...The survival rate is close to 80%, and it is directly related to the severity of the associated anomalies, as infants with isolated omphalocele have
Omphalocele is a rare congenital abdominal wall defect with a reported prevalence of 3.38 per 10,000 pregnancies. ...The survival rat
ERNICA evidence based guideline on omphalocele.
Irvine W, Kamp LMV, Spivack O, Wijnen R, Sgrò A, Brendel J, Zahn K, Matthyssens L, Gustafsson E, Røkkum H, Migliazza L, Sfeir R, Mutanen A, Rolle U, Dariel A, Miserez M, Lukosiute-Urboniene A, Vivanti A, Peters N, Conner P, Machtejevienė E, Russo F, Torres AS, Kokešová A, Stensvold HJ, Kipfmueller F, Boukhris MR, Tognon C, Eaton S, den Uijl I, Benachi A, Burgos CM. Irvine W, et al. Orphanet J Rare Dis. 2026 Mar 7. doi: 10.1186/s13023-026-04293-7. Online ahead of print. Orphanet J Rare Dis. 2026. PMID: 41794806 Free article. Review. No abstract available.
Giant Omphalocele: Systematic Review of Pulmonary Complications and Implications for Neonatal Care.
Peixoto J, Neto J, Pissarra S, Azevedo I, Soares H, Amaral R, Rocha G. Peixoto J, et al. Eur J Pediatr Surg. 2026 Apr;36(2):150-156. doi: 10.1055/a-2649-0781. Epub 2025 Jul 17. Eur J Pediatr Surg. 2026. PMID: 40675190
The primary objectives were to know the prevalences of pulmonary hypoplasia (PH), persistent pulmonary hypertension of the newborn (PPHN), and mortality in newborn infants with giant omphalocele (GO). A secondary aim was to assess the prevalence of syndromes and other cong …
The primary objectives were to know the prevalences of pulmonary hypoplasia (PH), persistent pulmonary hypertension of the newborn (PPHN), a …
European Paediatric Surgeons' Association Consensus Statement on the Management of Giant Omphalocele.
Saxena AK, Hayward RK, Mutanen A, Goneidy A, Ghattaura H, Gorter R, Weijnen R, Keijzer R, Soyer T; European Pediatric Surgeons' Association. Saxena AK, et al. Eur J Pediatr Surg. 2025 Oct;35(5):407-416. doi: 10.1055/a-2590-5592. Epub 2025 May 19. Eur J Pediatr Surg. 2025. PMID: 40389219
Giant omphalocele management had not reached a consensus from the pediatric surgical perspective regarding conservative treatments, surgical approaches, and clinical outcomes. ...Comments from participants were accounted to formulate the final consensus statement.Giant …
Giant omphalocele management had not reached a consensus from the pediatric surgical perspective regarding conservative treatments, s …
Unraveling the genetic basis of omphalocele: A systematic review.
Bousquet M, Le Guillou X, Jeanne M, Gazel P, Mitanchez D, Binet A. Bousquet M, et al. J Pediatr Surg. 2026 Feb 14;61(5):163015. doi: 10.1016/j.jpedsurg.2026.163015. Online ahead of print. J Pediatr Surg. 2026. PMID: 41698527 Review.
INTRODUCTION: Omphalocele is one of the most common congenital defects of the abdominal wall. Although a genetic contribution is strongly suspected, the underlying mechanisms remain poorly understood. The aim of this study was to systematically review and analyze genes pot …
INTRODUCTION: Omphalocele is one of the most common congenital defects of the abdominal wall. Although a genetic contribution is stro …
Haploinsufficiency of ABL1 is associated with dominant isolated omphalocele.
Kolvenbach CM, Yilmaz Ö, Lopes FM, Kalanithy JC, Lemberg K, Sharma V, Majmundar AJ, Geyer M, Woolf AS, Hildebrandt F, Odermatt B, Reutter H. Kolvenbach CM, et al. Front Cell Dev Biol. 2025 Aug 6;13:1630894. doi: 10.3389/fcell.2025.1630894. eCollection 2025. Front Cell Dev Biol. 2025. PMID: 40843169 Free PMC article.
Omphalocele is a rare birth defect of the abdominal wall that results in herniation of the visceral organs through the umbilicus. To date, there are no identified genetic causes for non-syndromic isolated omphalocele. Exome sequencing in a four-generation multiplex
Omphalocele is a rare birth defect of the abdominal wall that results in herniation of the visceral organs through the umbilicus. To
Gastroschisis.
Rentea RM, Gupta V. Rentea RM, et al. 2023 Apr 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 Apr 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 32491817 Free Books & Documents.
Compared with other abdominal wall defects diagnosed prenatally, such as omphalocele, only 10 percent of cases with gastroschisis are associated with malformations outside of the gastrointestinal tract. ...
Compared with other abdominal wall defects diagnosed prenatally, such as omphalocele, only 10 percent of cases with gastroschisis are …
Prospective outlook on negative pressure wound therapy (NPWT) for gastroschisis and ruptured omphalocele: A scoping review.
Kloping NA, Barmadisatrio. Kloping NA, et al. Med J Malaysia. 2025 Dec;80(Suppl 7):69-80. Med J Malaysia. 2025. PMID: 41451725 Free article.
INTRODUCTION: In cases of gastroschisis and ruptured omphalocele where primary closure is not feasible, physicians must employ alternative strategies to gradually reduce the herniated contents and promote epithelialization, either through non-surgical methods or with surgi …
INTRODUCTION: In cases of gastroschisis and ruptured omphalocele where primary closure is not feasible, physicians must employ altern …
FLNB-Related Disorders.
Robertson S, Meira J. Robertson S, et al. 2008 Oct 9 [updated 2025 Sep 11]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. 2008 Oct 9 [updated 2025 Sep 11]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. PMID: 20301736 Free Books & Documents. Review.
Occasional features include cleft palate, omphalocele, and cardiac and genitourinary anomalies. In individuals with FLNB-AO3, survival beyond the neonatal period is possible with intensive and invasive respiratory support. ...
Occasional features include cleft palate, omphalocele, and cardiac and genitourinary anomalies. In individuals with FLNB-AO3, surviva …
Neonatal Anesthesia.
Boyer TJ, Kritzmire SM. Boyer TJ, et al. 2023 Apr 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 Apr 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 31082074 Free Books & Documents.
Some babies are born with problems that put them at risk for needing imaging or surgical procedures early in life, such as tracheoesophageal fistula, congenital diaphragmatic hernia, gastroschisis, omphalocele, and pyloric stenosis. There are about 40,000 infants born wit …
Some babies are born with problems that put them at risk for needing imaging or surgical procedures early in life, such as tracheoesophageal …
103 results