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Survival of children with rare structural congenital anomalies: a multi-registry cohort study

Autor: Coi, Alessio, Santoro, Michele, Pierini, Anna, Rankin, Judith, Glinianaia, Svetlana V., Tan, Joachim, Reid, Abigail-Kate, Garne, Ester, Loane, Maria, Given, Joanne, Ballardini, Elisa, Cavero-Carbonell, Clara, de Walle, Hermien E.K., Gatt, Miriam, García-Villodre, Laura, Gissler, Mika, Jordan, Sue, Kiuru-Kuhlefelt, Sonja, Kjaer Urhoj, Stine, Klungsøyr, Kari, Lelong, Nathalie, Lutke, L. Renée, Neville, Amanda J., Rahshenas, Makan, Scanlon, Ieuan, Wellesley, Diana, Morris, Joan K.

Externí odkaz: https://hdl.handle.net/11250/3009090

Survival of children with rare structural congenital anomalies: a multi-registry cohort study.

Autor: Coi A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Via Moruzzi 1, 56124, Pisa, Italy. alessio.coi@ifc.cnr.it., Santoro M; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Via Moruzzi 1, 56124, Pisa, Italy., Pierini A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Via Moruzzi 1, 56124, Pisa, Italy.; Fondazione Toscana Gabriele Monasterio, Pisa, Italy., Rankin J; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Glinianaia SV; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Tan J; Population Health Research Institute, St George's University of London, London, UK., Reid AK; Population Health Research Institute, St George's University of London, London, UK., Garne E; Paediatric Department, Hospital Lillebaelt, Kolding, Denmark., Loane M; Faculty of Life and Health Sciences, Ulster University, Belfast, Northern Ireland, UK., Given J; Faculty of Life and Health Sciences, Ulster University, Belfast, Northern Ireland, UK., Ballardini E; Neonatal Intensive Care Unit, Paediatric Section, IMER Registry (Emilia Romagna Registry of Birth Defects), Department of Medical Sciences, University of Ferrara, Ferrara, Italy., Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain., de Walle HEK; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Gatt M; Malta Congenital Anomalies Register, Directorate of Health Information and Research, Pieta, Malta., García-Villodre L; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain., Gissler M; Information Services Department, THL Finnish Institute for Health and Welfare, Helsinki, Finland., Jordan S; Faculty of Medicine, Health and Life Science, Swansea University, Swansea, Wales, UK., Kiuru-Kuhlefelt S; Information Services Department, THL Finnish Institute for Health and Welfare, Helsinki, Finland., Kjaer Urhoj S; Paediatric Department, Hospital Lillebaelt, Kolding, Denmark.; Section of Epidemiology, Department of Public Health, University of Copenhagen, Copenhagen, Denmark., Klungsøyr K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.; Division for Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway., Lelong N; Center of Research in Epidemiology and StatisticS/CRESS/Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA, Université de Paris, Paris, France., Lutke LR; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Neville AJ; IMER Registry (Emila Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara Azienda Ospedaliero- Universitaria di Ferrara, Ferrara, Italy., Rahshenas M; Center of Research in Epidemiology and StatisticS/CRESS/Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), INSERM, INRA, Université de Paris, Paris, France., Scanlon I; Faculty of Medicine, Health and Life Science, Swansea University, Swansea, Wales, UK., Wellesley D; Wessex Clinical Genetics Service, Princess Anne Hospital, Faculty of Medicine, University Hospital Southampton, Southampton, UK., Morris JK; Population Health Research Institute, St George's University of London, London, UK.

Publikováno v: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Mar 29; Vol. 17 (1), pp. 142. Date of Electronic Publication: 2022 Mar 29.