Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders
Abstract Background 22q11.2 deletion syndrome (22q11DS) is a common recurrent neurogenetic condition associated with elevated risk for developmental neuropsychiatric disorders and intellectual disability. Children and adults with 22q11DS often exhibit marked social impairment as well as neurocogniti...
Main Authors: | Rhideeta Jalal, Aarti Nair, Amy Lin, Ariel Eckfeld, Leila Kushan, Jamie Zinberg, Katherine H. Karlsgodt, Tyrone D. Cannon, Carrie E. Bearden |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2021-04-01
|
Series: | Journal of Neurodevelopmental Disorders |
Subjects: | |
Online Access: | https://doi.org/10.1186/s11689-021-09363-4 |
Similar Items
-
Relationship between intelligence quotient measures and computerized neurocognitive performance in 22q11.2 deletion syndrome
by: Ruben C. Gur, et al.
Published: (2021-08-01) -
Case report: Novel phenotype in central 22q11.2 deletion syndrome
by: Patrick Dideum, et al.
Published: (2020-12-01) -
Palatoschisis, Schizophrenia and Hypocalcaemia: Phenotypic Expression of 22q11.2 Deletion Syndrome (DiGeorge Syndrome) in an Adult
by: Melissa Elise van der Meijs, et al.
Published: (2021-04-01) -
Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies
by: Paula Sandrin-Garcia, et al.
Published: (2007-01-01) -
22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment
by: Leyla S. Namazova-Baranova, et al.
Published: (2016-12-01)