Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

PURPOSE OF REVIEW: The 22q11.2 deletion syndrome (22q11DS) is associated with a broad spectrum of neurodevelopmental phenotypes and is the strongest known single genetic risk factor for schizophrenia. Compared to other rare structural pathogenic genetic variants, 22q11DS is relatively common and one...

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Detalles Bibliográficos
Autores principales: Fiksinski, Ania M., Schneider, Maude, Zinkstok, Janneke, Baribeau, Danielle, Chawner, Samuel J. R. A., Vorstman, Jacob A. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Child and Adolescent Disorders (TD Benton, Section Editor)
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904715/
https://www.ncbi.nlm.nih.gov/pubmed/33625600
http://dx.doi.org/10.1007/s11920-021-01225-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904715/
https://www.ncbi.nlm.nih.gov/pubmed/33625600
http://dx.doi.org/10.1007/s11920-021-01225-z

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