Cargando…

Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment

BACKGROUND: Previous investigations of individuals with chromosome 22q11.2 deletion syndrome (DS22q11.2) have reported alterations in both brain anatomy and cognitive function. Neuroanatomical studies have reported multiple abnormalities including changes in both gray and white matter in the tempora...

Descripción completa

Detalles Bibliográficos
Autores principales:	DeBoer, Tracy, Wu, Zhongle, Lee, Aaron, Simon, Tony J
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2007
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173902/ https://www.ncbi.nlm.nih.gov/pubmed/17956622 http://dx.doi.org/10.1186/1744-9081-3-54

Ejemplares similares

Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome
por: Simon, Tony J, et al.
Publicado: (2008)

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
por: Heung, Tracy, et al.
Publicado: (2022)

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
por: Cabaral, Margarita H, et al.
Publicado: (2012)

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome
por: Shapiro, Heather M., et al.
Publicado: (2014)

Clinical variability of chromosome 22q11.2 deletion syndrome
por: Boyarchuk, Oksana, et al.
Publicado: (2017)

Dopaminergic neurons in chromosome 22q11.2 deletion syndrome
por: Inoue, Haruhisa
Publicado: (2021)

Tonsillectomy in Children with 22q11.2 Deletion Syndrome
por: Arganbright, Jill M., et al.
Publicado: (2022)

Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome
por: Stoddard, Joel, et al.
Publicado: (2010)

2117: Parenting, anxiety, and adaptive function in children with chromosome 22q11.2 deletion syndrome
por: Angkustsiri, Kathleen, et al.
Publicado: (2018)

Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome
por: McGinn, Daniel E., et al.
Publicado: (2022)

Case Report: Autoimmune Psychosis in Chromosome 22q11.2 Deletion Syndrome
por: Ciano-Petersen, Nicolás Lundahl, et al.
Publicado: (2021)

Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome
por: Palmer, Lisa D., et al.
Publicado: (2022)

Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes
por: Quintero, Andrea I, et al.
Publicado: (2014)

Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size
por: Halder, Ashutosh, et al.
Publicado: (2012)

Thrombocytopenia and Postpartum Hemorrhage in a Woman with Chromosome 22q11.2 Deletion Syndrome
por: Pachtman, Sarah L., et al.
Publicado: (2016)

Chromosome 22q11.2 deletion causes PERK-dependent vulnerability in dopaminergic neurons
por: Arioka, Yuko, et al.
Publicado: (2020)

How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?
por: Beaton, Elliott A., et al.
Publicado: (2010)

Hematological abnormalities and 22q11.2 deletion syndrome
por: Rosa, Rafael Fabiano Machado, et al.
Publicado: (2011)

Obesity in adults with 22q11.2 deletion syndrome
por: Voll, S, et al.
Publicado: (2016)

Risk of malignancy in 22q11.2 deletion syndrome
por: Stevens, Toer, et al.
Publicado: (2017)

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
por: Du, Qiumei, et al.
Publicado: (2020)

Complement Activation in 22q11.2 Deletion Syndrome
por: Grinde, Dina, et al.
Publicado: (2020)

Laryngeal web with 22q11.2 deletion syndrome
por: Abe, Yasuhiro, et al.
Publicado: (2022)

A Cross-Sectional Analysis of the Development of Response Inhibition in Children with Chromosome 22q11.2 Deletion Syndrome
por: Shapiro, Heather M., et al.
Publicado: (2013)

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
por: Schonherz, Yael, et al.
Publicado: (2014)

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR
por: Hwang, Vicki J, et al.
Publicado: (2014)

Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome
por: Colarusso, Gloria, et al.
Publicado: (2010)

Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and Management
por: Biggs, Sarah E., et al.
Publicado: (2023)

Detection of 21q11.2‐q22.11 deletions in a fetus by NIPT
por: Zheng, Yunyun, et al.
Publicado: (2019)

Evaluation of 22q11.2 deletion in Cleft Palate patients
por: Prabodha, L. B. Lahiru, et al.
Publicado: (2012)

Genotype-phenotype correlation in 22q11.2 deletion syndrome
por: Michaelovsky, Elena, et al.
Publicado: (2012)

Psychopathology and cognition in children with 22q11.2 deletion syndrome
por: Niarchou, Maria, et al.
Publicado: (2014)

Otologic and audiologic findings in 22q11.2 deletion syndrome
por: Verheij, E., et al.
Publicado: (2016)

Psychiatric Disorders Associated with 22q11.2 Deletion Syndrome
por: Gambini, Orsola
Publicado: (2016)

Disrupted anatomic networks in the 22q11.2 deletion syndrome
por: Schmitt, J. Eric, et al.
Publicado: (2016)

Visual processing deficits in 22q11.2 Deletion Syndrome
por: Biria, Marjan, et al.
Publicado: (2017)

22q11.2 Deletion Syndrome–Associated Parkinson's Disease
por: Boot, Erik, et al.
Publicado: (2018)

22q11.2 Deletion and Duplication Syndromes and COVID-19
por: Crowley, T. Blaine, et al.
Publicado: (2022)

Deletion Syndrome 22q11.2: A Systematic Review
por: Cortés-Martín, Jonathan, et al.
Publicado: (2022)

Clinical management of psychosis in 22q11.2 deletion syndrome
por: Iftimovici, Anton, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_tgl9ohit5qukft8d0s356lgfbh