Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology

Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology

Stress and anxiety negatively impact the working memory system by competing for executive resources. Broad memory deficits have been reported in individuals with chromosome 22q11.2 deletion syndrome (22q11.2DS). We investigated anxiety and physiological stress reactivity in relation to visuospatial...

Full description

Bibliographic Details
Main Author:	Sanders, Ashley F. P.
Format:	Others
Published:	ScholarWorks@UNO 2016
Subjects:	Anxiety Chromosome 22q11.2 Deletion Syndrome DiGeorge Stress Velocardiofacial Syndrome Working Memory Biological Psychology Child Psychology Cognitive Neuroscience Developmental Neuroscience
Online Access:	http://scholarworks.uno.edu/td/2191 http://scholarworks.uno.edu/cgi/viewcontent.cgi?article=3277&context=td

Similar Items

Immune Defects in Chromosome 22q11.2 Deletion Syndromes
by: Bobey, Nicola A.
Published: (2010)

Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome
by: Kathleen Rooney, et al.
Published: (2021-08-01)

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
by: Cabaral Margarita H, et al.
Published: (2012-04-01)

A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome
by: Raad A. Haddad, et al.
Published: (2019-08-01)

Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome
by: Gloria Colarusso, et al.
Published: (2010-06-01)

Obstructive sleep apnea syndrome in children with 22q11.2 deletion syndrome after operative intervention for velopharyngeal insufficiency
by: David Jeffrey Crockett, et al.
Published: (2014-08-01)

Familial 22q11.2 deletion syndrome with autosomal dominant inheritance
by: Bahar Gokturk, et al.
Published: (2016-06-01)

Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate
by: Narges Nouri, et al.
Published: (2016-01-01)

Síndrome de deleção 22q11.2: importância da avaliação clínica e técnica de FISH 22q11.2 deletion syndrome: importance of clinical evaluation and FISH analysis
by: Dayane Bohn Koshiyama, et al.
Published: (2009-01-01)

Síndrome de deleção 22q11.2: compreendendo o CATCH22 22q11.2 deletion syndrome: catching the CATCH22
by: Rafael Fabiano M. Rosa, et al.
Published: (2009-06-01)

22q11.2 deletion (DiGeorge) syndrome: a mother’s open letter
by: Antonio Baldini, et al.
Published: (2011-07-01)

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)

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
by: Qiumei Du, et al.
Published: (2020-02-01)

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)

High specificity PCR screening for 22q11.2 microdeletion in three different ethnic groups
by: A.C. Pereira, et al.
Published: (2003-10-01)

Structural connectivity and immunological correlates of emotion processing in children with chromosome 22q11.2 deletion syndrome
by: Sanders, Ashley F. P.
Published: (2019)

Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis
by: M. Fernanda Rozas, et al.
Published: (2019-08-01)

Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother
by: Chih-Ping Chen, et al.
Published: (2021-01-01)

An interictal schizophrenia-like psychosis in an adult patient with 22q11.2 deletion syndrome
by: Yasutaka Tastuzawa, et al.
Published: (2015-01-01)

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome
by: Lauren Welby, et al.
Published: (2020-01-01)

MicroRNA dysregulation, gene networks and risk for schizophrenia in 22q11.2 deletion syndrome
by: Daniele eMerico, et al.
Published: (2014-11-01)

The Barriers and Quality of Care Issues for Individuals Diagnosed with 22q11.2 Deletion Syndrome
by: Miller, Barbara Bavette
Published: (2017)

Acute dystonia in a patient with 22q11.2 deletion syndrome
by: Konstantinos Kontoangelos, et al.
Published: (2015-09-01)

Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?
by: Li Deling, et al.
Published: (2012-04-01)

Increased Medical Interventions in Children with 22q11.2 Deletion Syndrome (Velocardiofacial Syndrome)
by: King, Emily
Published: (2011)

22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment
by: Leyla S. Namazova-Baranova, et al.
Published: (2016-12-01)

DiGeorge Syndrome: a not so rare disease
by: Angela BF Fomin, et al.
Published: (2010-01-01)

Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus
by: Dong-Yoon Yoo, et al.
Published: (2017-06-01)

22q11.2 DELETION SYNDROME: ALGORITHM FOR THE EARLY DIAGNOSIS AND TREATMENT
by: Leyla S. Namazova-Baranova, et al.
Published: (2017-11-01)

Chromosome 22q11.2 deletion: world definition criteria, standards for diagnosis and monitoring
by: M.A. Gonchar, et al.
Published: (2018-02-01)

Examining the Relationship Between Parenting Stress and Anxiety in Children with 22q11.2 Deletion Syndrome
by: Berton, Jacquelynn
Published: (2019)

Hematological abnormalities and 22q11.2 deletion syndrome
by: Rafael Fabiano Machado Rosa, et al.
Published: (2011-01-01)

Hipocalcemia Neonatal e Baixa Estatura por Delecção em 2411 2
by: Jorge M. Saraiva, et al.
Published: (2014-09-01)

Optimisation de la différenciation neuronale et musculaire de cellules pluripotentes induites humaines pour la modélisation des maladies rares : exemple du syndrome de DiGeorge
by: Badja, Cherif
Published: (2015)

Síndrome de deleção 22q11.2 e cardiopatias congênitas 22q11.2 deletion syndrome and congenital heart defects
by: Rafael Fabiano M. Rosa, et al.
Published: (2011-06-01)

Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome
by: Beverly A. Karpinski, et al.
Published: (2014-02-01)

Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women
by: Kuntharee Traisrisilp, et al.
Published: (2020-05-01)

Platybasia in 22q11.2 Deletion Syndrome Is Not Correlated with Speech Resonance
by: Nicole E Spruijt, et al.
Published: (2014-07-01)

Current perspectives on velocardiofacial syndrome
by: Saikrishna Lakkakula, et al.
Published: (2017-01-01)

RETROSPECTIVE CHART REVIEW OF HOSPITALIZATIONS AND HEALTH PROBLEMS OF CHILDREN WITH VELOCARDIOFACIAL SYNDROME
by: WOJTASIAK, MICHELLE LEA
Published: (2002)