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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.
Boot, Erik; Óskarsdóttir, Sólveig; Loo, Joanne C Y; Crowley, Terrence Blaine; Orchanian-Cheff, Ani; Andrade, Danielle M; Arganbright, Jill M; Castelein, René M; Cserti-Gazdewich, Christine; de Reuver, Steven; Fiksinski, Ania M; Klingberg, Gunilla; Lang, Anthony E; Mascarenhas, Maria R; Moss, Edward M; Nowakowska, Beata Anna; Oechslin, Erwin; Palmer, Lisa; Repetto, Gabriela M; Reyes, Nikolai Gil D; Schneider, Maude; Silversides, Candice; Sullivan, Kathleen E; Swillen, Ann; van Amelsvoort, Therese A M J; Van Batavia, Jason P; Vingerhoets, Claudia; McDonald-McGinn, Donna M; Bassett, Anne S.
Afiliación
  • Boot E; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands. Electronic address: erik.bo
  • Óskarsdóttir S; Department of Pediatric Rheumatology and Immunology, Queen Silvia Children's Hospital, Sahlgrenska University Hospital, Gothenburg, Sweden; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. Electronic address: solveig.oskarsd
  • Loo JCY; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
  • Crowley TB; 22q and You Center, Clinical Genetics Center, and Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Orchanian-Cheff A; Library and Information Services, and The Institute of Education Research (TIER), University Health Network, Toronto, Ontario, Canada.
  • Andrade DM; Adult Genetic Epilepsy Program, Toronto Western Hospital and University of Toronto, Toronto, Ontario, Canada.
  • Arganbright JM; Division of Otolaryngology, Children's Mercy Hospital and University of Missouri Kansas City School of Medicine, Kansas City, MO.
  • Castelein RM; Department of Orthopedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Cserti-Gazdewich C; Hematology and Transfusion Medicine, University Health Network, Toronto, Ontario, Canada.
  • de Reuver S; Department of Orthopedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Fiksinski AM; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands; Department of Pediatric Psychology, University Medical Centre, Wilhelmina Children's Hospital, Utrecht, The Netherlands.
  • Klingberg G; Faculty of Odontology, Malmö University, Malmö, Sweden.
  • Lang AE; The Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
  • Mascarenhas MR; Division of Gastroenterology and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA.
  • Moss EM; Bryn Mawr, PA.
  • Nowakowska BA; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.
  • Oechslin E; Toronto Adult Congenital Heart Disease Program, Peter Munk Cardiac Centre, University Health Network and University of Toronto, Toronto, Ontario, Canada.
  • Palmer L; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
  • Repetto GM; Rare Diseases Program, Institute for Sciences and Innovation in Medicine, Facultad de Medicina Clinica Alemana Universidad del Desarrollo, Santiago, Chile.
  • Reyes NGD; The Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders, Toronto Western Hospital, University Health Network, Toronto, Ontario, Canada.
  • Schneider M; Clinical Psychology Unit for Intellectual and Developmental Disabilities, Faculty of Psychology and Educational Sciences, University of Geneva, Geneva, Switzerland.
  • Silversides C; Toronto ACHD Program, Mount Sinai and Toronto General Hospitals, University of Toronto, Toronto, Ontario, Canada.
  • Sullivan KE; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA; Division of Allergy and Immunology and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Swillen A; Center for Human Genetics, University Hospital UZ Leuven, Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • van Amelsvoort TAMJ; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands.
  • Van Batavia JP; Department of Surgery, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA; Division of Urology and 22q and You Center, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Vingerhoets C; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands.
  • McDonald-McGinn DM; 22q and You Center, Clinical Genetics Center, and Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA; Department of Human Biology and Medical Genetics, Sapienza U
  • Bassett AS; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada; Clinical Genetics Research Program and Campbell Family Mental Health Research Institute, Centre for Addiction and
Genet Med ; 25(3): 100344, 2023 03.
Article en En | MEDLINE | ID: mdl-36729052
This review aimed to update the clinical practice guidelines for managing adults with 22q11.2 deletion syndrome (22q11.2DS). The 22q11.2 Society recruited expert clinicians worldwide to revise the original clinical practice guidelines for adults in a stepwise process according to best practices: (1) a systematic literature search (1992-2021), (2) study selection and synthesis by clinical experts from 8 countries, covering 24 subspecialties, and (3) formulation of consensus recommendations based on the literature and further shaped by patient advocate survey results. Of 2441 22q11.2DS-relevant publications initially identified, 2344 received full-text review, with 2318 meeting inclusion criteria (clinical care relevance to 22q11.2DS) including 894 with potential relevance to adults. The evidence base remains limited. Thus multidisciplinary recommendations represent statements of current best practice for this evolving field, informed by the available literature. These recommendations provide guidance for the recognition, evaluation, surveillance, and management of the many emerging and chronic 22q11.2DS-associated multisystem morbidities relevant to adults. The recommendations also address key genetic counseling and psychosocial considerations for the increasing numbers of adults with this complex condition.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Límite: Adult / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Tipo de estudio: Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Límite: Adult / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos