Literature DB >> 24214349

3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.

Santina Città1, Serafino Buono, Donatella Greco, Concetta Barone, Enrico Alfei, Sara Bulgheroni, Arianna Usilla, Chiara Pantaleoni, Corrado Romano.   

Abstract

The 3q29 microdeletion syndrome is a rare, recurrent genomic disorder, associated with a variable phenotype, despite the same deletion size, consisting in neurodevelopmental features, such as intellectual disability (ID), schizophrenia, autism, bipolar disorder, depression and mild facial morphological anomalies/congenital malformations. A thorough neuropsychiatric evaluation has never been reported in patients with such syndrome. We analyzed the clinical phenotype of four individuals with 3q29 microdeletion syndrome, with special emphasis on the cognitive and behavioral assessment, in order to delineate the neuropsychiatric phenotype related to this condition. We assessed these patients with standardized scales or checklists measuring the cognitive (WISC III or LIPS-R), behavioral (CBCL) and adaptive (VABS) performances. An accurate evaluation in our sample highlights different degrees of ID, variable behavioral disorders, and a preservation of communicative skills among remaining adaptive areas, as the neuropsychiatric hallmark of 3q29 microdeletion syndrome.
© 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  3q29 microdeletion syndrome; behavioral phenotype; cognitive phenotype

Mesh:

Year:  2013        PMID: 24214349     DOI: 10.1002/ajmg.a.36142

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  7 in total

Review 1.  A clinical case report and literature review of the 3q29 microdeletion syndrome.

Authors:  Devin M Cox; Merlin G Butler
Journal:  Clin Dysmorphol       Date:  2015-07       Impact factor: 0.816

2.  Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study.

Authors:  Ye Cao; Zhihua Li; Jill A Rosenfeld; Amber N Pursley; Ankita Patel; Jin Huang; Huilin Wang; Min Chen; Xiaofang Sun; Tak Yeung Leung; Sau Wai Cheung; Kwong Wai Choy
Journal:  Genet Med       Date:  2016-02-25       Impact factor: 8.822

3.  Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case series.

Authors:  Eva Albertsen Malt; Katalin Juhasz; Anna Frengen; Teresia Wangensteen; Nina Merete Emilsen; Borre Hansen; Oleg Agafonov; Hilde Loge Nilsen
Journal:  Mol Genet Genomic Med       Date:  2019-07-25       Impact factor: 2.183

4.  Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.

Authors:  Rebecca M Pollak; Melissa M Murphy; Michael P Epstein; Michael E Zwick; Cheryl Klaiman; Celine A Saulnier; Jennifer G Mulle
Journal:  Mol Autism       Date:  2019-07-16       Impact factor: 7.509

5.  Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report.

Authors:  Melissa M Murphy; T Lindsey Burrell; Joseph F Cubells; Michael T Epstein; Roberto Espana; Michael J Gambello; Katrina Goines; Cheryl Klaiman; Sookyong Koh; Rossana Sanchez Russo; Celine A Saulnier; Elaine Walker; Jennifer Gladys Mulle
Journal:  BMC Psychiatry       Date:  2020-04-22       Impact factor: 3.630

Review 6.  Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review.

Authors:  Fagui Yue; Shu Deng; Qi Xi; Yuting Jiang; Jing He; Hongguo Zhang; Ruizhi Liu
Journal:  Medicine (Baltimore)       Date:  2021-01-08       Impact factor: 1.817

7.  Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.

Authors:  Megan R Glassford; Jill A Rosenfeld; Alexa A Freedman; Michael E Zwick; Jennifer G Mulle
Journal:  Am J Med Genet A       Date:  2016-01-06       Impact factor: 2.802

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.