Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome

Journal
Genetics in Medicine
ISSN
1098-3600
Date Issued
2023
Author(s)
Erik Boot
Sólveig Óskarsdóttir
Joanne C.Y. Loo
Terrence Blaine Crowley
Ani Orchanian-Cheff
Danielle M. Andrade
Jill M. Arganbright
René M. Castelein
Christine Cserti-Gazdewich
Steven de Reuver
Ania M. Fiksinski
Gunilla Klingberg
Anthony E. Lang
Maria R. Mascarenhas
Edward M. Moss
Beata Anna Nowakowska
Erwin Oechslin
Lisa Palmer
Nikolai Gil D. Reyes
Maude Schneider
Candice Silversides
Kathleen E. Sullivan
Ann Swillen
Therese A.M.J. van Amelsvoort
Jason P. Van Batavia
Claudia Vingerhoets
Donna M. McDonald-McGinn
Anne S. Bassett
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85146756051
WoS ID
WOS:001049076000001
DOI
URL
URL Institutional Repository
Cite this document
Boot, E., Óskarsdóttir, S., Loo, J. C. Y., Crowley, T. B., Orchanian-Cheff, A., Andrade, D. M., Arganbright, J. M., Castelein, R. M., Cserti-Gazdewich, C., De Reuver, S., Fiksinski, A. M., Klingberg, G., Lang, A. E., Mascarenhas, M. R., Moss, E. M., Nowakowska, B. A., Oechslin, E., Palmer, L., Repetto, G. M., … Bassett, A. S. (2023). Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine, 25(3), 100344. https://doi.org/10.1016/j.gim.2022.11.012
Subjects
adults

; 

aging

; 

clinical practice guidelines

; 

digeorge syndrome

; 

treatment

; 

adult

; 

clinical relevance

; 

consensus

; 

digeorge syndrome

; 

genetic counseling

; 

humans

; 

surveys and questionnaires

; 

antidepressant agent

; 

anxiolytic agent

; 

calcium

; 

clozapine

; 

neuroleptic agent

; 

vitamin d

; 

22q11.2 deletion syndrome

; 

adulthood

; 

aging

; 

anxiety disorder

; 

asthma

; 

autoimmune disease

; 

brain dysfunction

; 

chromosome deletion

; 

cognition

; 

depression

; 

disease management

; 

evidence based practice

; 

fluorescence in situ hybridization

; 

gastrointestinal disease

; 

general surgery

; 

genetic counseling

; 

genetic screening

; 

gynecologic disease

; 

human

; 

hypocalcemia

; 

hypothyroidism

; 

ischemic heart disease

; 

mental disease

; 

microarray analysis

; 

multiplex ligation dependent probe amplification

; 

practice guideline

; 

preimplantation genetic diagnosis

; 

prognosis

; 

psychosis

; 

review

; 

schizophrenia

; 

sensory dysfunction

; 

sexual health

; 

skin disease

; 

sleep disordered breathing

; 

systematic review

; 

thrombocytopenia

; 

tooth disease

; 

transitional care

; 

urogenital tract disease

; 

adult

; 

consensus

; 

digeorge syndrome

; 

genetics

; 

questionnaire