Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

van de Putte, R; van Rooij, IALM; Marcelis, CLM; Guo, M; Brunner, HG; Addor, MC; Cavero-Carbonell, C; Dias, CM; Draper, ES; Etxebarriarteun, L; Gatt, M; Haeusler, M; Khoshnood, B; Klungsoyr, K; Kurinczuk, JJ; Lanzoni, M; Latos-Bielenska, A; Luyt, K; O'Mahony, MT; Miller, N; Mullaney, C; Nelen, V; Neville, AJ; Perthus, I; Pierini, A; Randrianaivo, H; Rankin, J; Rissmann, A; Rouget, F; Schaub, B; Tucker, D; Wellesley, D; Wiesel, A; Zymak-Zakutnia, N; Loane, M; Barisic, I; de Walle, HEK; Roeleveld, N; Bergman, JEH.
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study.
Pediatr Res. 2020; 87(3):541-549 Doi: 10.1038/s41390-019-0561-y [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

Co-authors Med Uni Graz
Haeusler Martin
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
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. 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. 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. The clearly defined VACTERL component features and the VACTERL subtypes introduced will improve both clinical practice and etiologic research.
Find related publications in this database (using NLM MeSH Indexing)
Anal Canal - abnormalities
Consensus -
Databases, Factual -
Esophagus - abnormalities
Esophagus - epidemiology
Genetic Predisposition to Disease -
Heart Defects, Congenital - classification
Heart Defects, Congenital - diagnosis
Heart Defects, Congenital - epidemiology
Heart Defects, Congenital - genetics
Humans -
International Classification of Diseases -
Kidney - abnormalities
Limb Deformities, Congenital - classification
Limb Deformities, Congenital - diagnosis
Limb Deformities, Congenital - epidemiology
Limb Deformities, Congenital - genetics
Phenotype -
Predictive Value of Tests -
Prevalence -
Spine - abnormalities
Terminology as Topic -
Trachea - abnormalities

© Med Uni GrazImprint