Costello Syndrome: Clinical Phenotype, Genotype, and Management Guidelines
Received: 31 March 2019 Revised: 22 May 2019 Accepted: 1 June 2019 DOI: 10.1002/ajmg.a.61270 ORIGINAL ARTICLE Costello syndrome: Clinical phenotype, genotype, and management guidelines Karen W. Gripp1 | Lindsey A. Morse2 | Marni Axelrad3 | Kathryn C. Chatfield4 | Aaron Chidekel5 | William Dobyns6 | Daniel Doyle7 | Bronwyn Kerr8 | Angela E. Lin9 | David D. Schwartz3 | Barbara J. Sibbles10 | Dawn Siegel11 | Suma P. Shankar12 | David A. Stevenson13 | Mihir M. Thacker14 | K. Nicole Weaver15 | Sue M. White16 | Katherine A. Rauen12 1Division of Medical Genetics, Department of Pediatrics, A.I. duPont Hospital for Children, Wilmington, Delaware 2Ferre Institute, Binghamton, New York, New York 3Psychology Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas 4Section of Cardiology, Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado 5Division of Pulmonology, Department of Pediatrics, A.I. duPont Hospital for Children, Wilmington, Delaware 6Division of Medical Genetics, Seattle Children's Hospital, Seattle, Washington 7Division of Endocrinology, A.I. duPont Hospital for Children, Wilmington, Delaware 8Manchester Center for Genomic Medicine, University of Manchester, Manchester, UK 9Medical Genetics Unit, Department of Pediatrics, MassGeneral Hospital for Children, Boston, Massachusetts 10Division of Pediatrics, Erasmus MC-Sophia Children's Hospital, Rotterdam, the Netherlands 11Department of Dermatology, Medical College of Wisconsin, Milwaukee, Wisconsin 12Division of Genomic Medicine, Department
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