Pregled bibliografske jedinice broj: 1170239
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study // Pediatric Research, 87 (2019), 3; 541-549 doi:10.1038/s41390-019-0561-y (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1170239 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Spectrum of congenital anomalies among VACTERL cases: a
EUROCAT population-based study
Autori
Van de Putte, Romy ; van Rooij, Iris A. L. M. ; Marcelis, Carlo L. M. ; Guo, Michel ; Brunner, Han G. ; Addor, Marie-Claude ; Cavero- Carbonell, Clara ; Dias, Carlos M. ; Draper, Elizabeth S. ; Etxebarriarteun, Larraitz ; Gatt, Miriam ; Haeusler, Martin ; Khoshnood, Babak ; Klungsoyr, Kari ; Kurinczuk, Jenny J. ; Lanzoni, Monica ; Latos-Bielenska, Anna ; Luyt, Karen ; O’Mahony, Mary T. ; Miller, Nicola ; Mullaney, Carmel ; Nelen, Vera ; Neville, Amanda J. ; Perthus, Isabelle ; Pierini, Anna ; Randrianaivo, Hanitra ; Rankin, Judith ; Rissmann, Anke ; Rouget, Florence ; Schaub, Bruno ; Tucker, David ; Wellesley, Diana ; Wiesel, Awi ; Zymak-Zakutnia, Natalya ; Loane, Maria ; Barisic, Ingeborg ; de Walle, Hermien E. K. ; Roeleveld, Nel ; Bergman, Jorieke E. H.
Izvornik
Pediatric Research (0031-3998) 87
(2019), 3;
541-549
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
VACTERL ; associated anomalies ; epidemiology
Sažetak
Background: The VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association is the non-random occurrence of at least three of these congenital anomalies: vertebral, anal, cardiac, tracheo-esophageal, renal, and limb anomalies. Diagnosing VACTERL patients is difficult, as many disorders have multiple features in common with VACTERL. The aims of this study were to clearly outline component features, describe the phenotypic spectrum among the largest group of VACTERL patients thus far reported, and to identify phenotypically similar subtypes. Methods: A case-only study was performed assessing data on 501 cases recorded with VACTERL in the JRC-EUROCAT (Joint Research Centre-European Surveillance of Congenital Anomalies) central database (birth years: 1980-2015). We differentiated between major and minor VACTERL features and anomalies outside the VACTERL spectrum to create a clear definition of VACTERL. Results: In total, 397 cases (79%) fulfilled our VACTERL diagnostic criteria. The most commonly observed major VACTERL features were anorectal malformations and esophageal atresia/tracheo- esophageal fistula (both occurring in 62% of VACTERL cases), followed by cardiac (57%), renal (51%), vertebral (33%), and limb anomalies (25%), in every possible combination. Three VACTERL subtypes were defined: STRICT-VACTERL, VACTERL-LIKE, and VACTERL-PLUS, based on severity and presence of additional congenital anomalies. Conclusion: The clearly defined VACTERL component features and the VACTERL subtypes introduced will improve both clinical practice and etiologic research.
Izvorni jezik
Engleski
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE