Literature DB >> 18636636

The neurocognitive phenotype in velo-cardio-facial syndrome: a developmental perspective.

Kevin M Antshel1, Wanda Fremont, Wendy R Kates.   

Abstract

Although research has focused primarily on the wide range of variability in the cognitive phenotype between individuals with velo-cardio-facial syndrome (VCFS), we know relatively little about the extent to which within-individual expressions of the cognitive phenotype remain stable throughout development. General cognitive functioning in the low borderline range is the most consistent cognitive finding. Stronger reading decoding and spelling skills as well as auditory/verbal rote memory skills have been reported to be areas of relative strength. Conversely, significant visuospatial dysfunction, diminished math attainment, and executive dysfunction have all been reported as phenotypic. We propose several considerations that could advance our knowledge of developmental changes in the VCFS cognitive phenotype. The most salient of these is the need for more longitudinal designs with carefully matched control participants.

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Year:  2008        PMID: 18636636     DOI: 10.1002/ddrr.7

Source DB:  PubMed          Journal:  Dev Disabil Res Rev        ISSN: 1940-5529


  30 in total

1.  Subthreshold psychotic symptoms in 22q11.2 deletion syndrome.

Authors:  Sunny X Tang; James J Yi; Tyler M Moore; Monica E Calkins; Christian G Kohler; Daneen A Whinna; Margaret C Souders; Elaine H Zackai; Donna M McDonald-McGinn; Beverly S Emanuel; Warren B Bilker; Ruben C Gur; Raquel E Gur
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2014-06-19       Impact factor: 8.829

2.  White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosis.

Authors:  Wendy R Kates; Amy K Olszewski; Matthew H Gnirke; Zora Kikinis; Joshua Nelson; Kevin M Antshel; Wanda Fremont; Petya D Radoeva; Frank A Middleton; Martha E Shenton; Ioana L Coman
Journal:  Schizophr Res       Date:  2014-07-25       Impact factor: 4.939

3.  Neural substrates of inhibitory control deficits in 22q11.2 deletion syndrome.

Authors:  C A Montojo; M Jalbrzikowski; E Congdon; S Domicoli; C Chow; C Dawson; K H Karlsgodt; R M Bilder; C E Bearden
Journal:  Cereb Cortex       Date:  2013-10-31       Impact factor: 5.357

4.  Practical guidelines for managing patients with 22q11.2 deletion syndrome.

Authors:  Anne S Bassett; Donna M McDonald-McGinn; Koen Devriendt; Maria Cristina Digilio; Paula Goldenberg; Alex Habel; Bruno Marino; Solveig Oskarsdottir; Nicole Philip; Kathleen Sullivan; Ann Swillen; Jacob Vorstman
Journal:  J Pediatr       Date:  2011-05-12       Impact factor: 4.406

5.  The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome.

Authors:  Meghan Muldoon; Opal Y Ousley; Lisa J Kobrynski; Sheena Patel; Matthew E Oster; Samuel Fernandez-Carriba; Joseph F Cubells; Karlene Coleman; Bradley D Pearce
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2014-09-30       Impact factor: 5.270

6.  The use of two different MLPA kits in 22q11.2 deletion syndrome.

Authors:  L J M Evers; J J M Engelen; L M H Houben; L M G Curfs; T A M J van Amelsvoort
Journal:  Eur J Med Genet       Date:  2016-02-24       Impact factor: 2.708

7.  Childhood predictors of written expression in late adolescents with 22q11.2 deletion syndrome: a longitudinal study.

Authors:  N Hamsho; K M Antshel; T L Eckert; W R Kates
Journal:  J Intellect Disabil Res       Date:  2017-03-08

8.  Predicting reading comprehension academic achievement in late adolescents with velo-cardio-facial (22q11.2 deletion) syndrome (VCFS): a longitudinal study.

Authors:  K Antshel; B Hier; W Fremont; S V Faraone; W Kates
Journal:  J Intellect Disabil Res       Date:  2014-05-26

9.  Behavior, brain, and genome in genomic disorders: finding the correspondences.

Authors:  Elena L Grigorenko; Alexander E Urban; Einar Mencl
Journal:  J Dev Behav Pediatr       Date:  2010-09       Impact factor: 2.225

10.  White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis.

Authors:  Matthew D Perlstein; Moeed R Chohan; Ioana L Coman; Kevin M Antshel; Wanda P Fremont; Matthew H Gnirke; Zora Kikinis; Frank A Middleton; Petya D Radoeva; Martha E Shenton; Wendy R Kates
Journal:  Schizophr Res       Date:  2013-12-08       Impact factor: 4.939

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