Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement

被引:0
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作者
Antonie D. Kline
Joanna F. Moss
Angelo Selicorni
Anne-Marie Bisgaard
Matthew A. Deardorff
Peter M. Gillett
Stacey L. Ishman
Lynne M. Kerr
Alex V. Levin
Paul A. Mulder
Feliciano J. Ramos
Jolanta Wierzba
Paola Francesca Ajmone
David Axtell
Natalie Blagowidow
Anna Cereda
Antonella Costantino
Valerie Cormier-Daire
David FitzPatrick
Marco Grados
Laura Groves
Whitney Guthrie
Sylvia Huisman
Frank J. Kaiser
Gerritjan Koekkoek
Mary Levis
Milena Mariani
Joseph P. McCleery
Leonie A. Menke
Amy Metrena
Julia O’Connor
Chris Oliver
Juan Pie
Sigrid Piening
Carol J. Potter
Ana L. Quaglio
Egbert Redeker
David Richman
Claudia Rigamonti
Angell Shi
Zeynep Tümer
Ingrid D. C. Van Balkom
Raoul C. Hennekam
机构
[1] Greater Baltimore Medical Centre,Harvey Institute of Human Genetics
[2] University of Birmingham,Cerebra Centre for Neurodevelopmental Disorders, School of Psychology
[3] ASST Lariana,Department of Paediatrics, Presidio S. Femro
[4] Rigshospitalet,Kennedy Centre, Department of Paediatrics and Adolescent Medicine
[5] University of Pennsylvania Perelman School of Medicine,Division of Human Genetics, Children’s Hospital of Philadelphia, and Department of Pediatrics
[6] Royal Hospital for Sick Children,GI Department
[7] University of Cincinnati,Departments of Otolaryngology and Pulmonary Medicine, Cincinnati Children’s Hospital Medical Centre
[8] University of Utah Medical Centre,Division of Pediatric Neurology, Department of Paediatrics
[9] Thomas Jefferson University,Paediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital
[10] Lentis Psychiatric Institute,Jonx Department of Youth Mental Health and Autism
[11] University of Zaragoza,Unit of Clinical Genetics, Paediatrics, University Clinic Hospital ‘Lozano Blesa’ CIBERER
[12] Medical University of Gdansk,GCV02 and ISS
[13] Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico,Aragón, Department of Pharmacology
[14] CdLS Foundation UK and Ireland,Physiology and Paediatrics, School of Medicine
[15] Greater Baltimore Medical Center,Department of Paediatrics, Haematology and Oncology, Department of General Nursery
[16] ASST Papa Giovanni XXIII,Child and Adolescent Neuropsychiatric Unit
[17] Université Paris Descartes-Sorbonne Paris Cité,Harvey Institute of Human Genetics
[18] Hôpital Necker-Enfants Malades,Department of Paediatrics
[19] University of Edinburgh Western General Hospital,Department of Genetics, INSERM UMR1163
[20] John Hopkins University School of Medicine,Human Genetics Unit, Medical and Developmental Genetics
[21] Children’s Hospital of Philadelphia,Division of Child and Adolescent Psychiatry
[22] University of Amsterdam,Centre for Autism Research
[23] University of Lübeck,Department of Paediatrics, Academic Medical Centre
[24] CdLS World Federation’s,Section for Functional Genetics, Institute for Human Genetics
[25] Wicomico County Board of Education,Clinical Paediatric Genetics Unit, Paediatrics Clinics, MBBM Foundation
[26] S. Gerardo Hospital,Kennedy Krieger Institute
[27] Danbury Public Schools,Department of Gastroenterology
[28] Johns Hopkins School of Medicine,Genética Médica
[29] Nationwide Children’s,Department of Clinical Genetics, Academic Medical Centre
[30] Hospital del Este,Department of Educational Psychology and Leadership
[31] Eva Perón,Rob Giel Research Centre, Department of Psychiatry
[32] University of Amsterdam,undefined
[33] Texas Tech University,undefined
[34] The Sidney Kimmel Medical College of Thomas Jefferson University,undefined
[35] University Medical Centre Groningen,undefined
来源
Nature Reviews Genetics | 2018年 / 19卷
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摘要
Cornelia de Lange syndrome (CdLS) is an archetypical genetic syndrome that is characterized by intellectual disability, well-defined facial features, upper limb anomalies and atypical growth, among numerous other signs and symptoms. It is caused by variants in any one of seven genes, all of which have a structural or regulatory function in the cohesin complex. Although recent advances in next-generation sequencing have improved molecular diagnostics, marked heterogeneity exists in clinical and molecular diagnostic approaches and care practices worldwide. Here, we outline a series of recommendations that document the consensus of a group of international experts on clinical diagnostic criteria, both for classic CdLS and non-classic CdLS phenotypes, molecular investigations, long-term management and care planning.
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页码:649 / 666
页数:17
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