Literature DB >> 24722762

Brief report: functional MRI of a patient with 7q11.23 duplication syndrome and autism spectrum disorder.

Paolo Prontera1, Domenico Serino, Bernardo Caldini, Laura Scarponi, Giuseppe Merla, Giuseppe Testa, Marco Muti, Valerio Napolioni, Giovanni Mazzotta, Massimo Piccirilli, Emilio Donti.   

Abstract

The duplication of the Williams-Beuren syndrome (WBS) region (7q11.23) is a copy number variant associated with autism spectrum disorder (ASD). One of the most intriguing aspects is that the reciprocal microdeletion causes WBS, characterized by hypersociability, marked empathy, and a relative capacity in verbal short-term memory and language. Herein, we studied, by using functional morphological and volumetric magnetic resonance, a 17-year-old male patient who displays a de novo 7q11.23 duplication and ASD. The limbic system of the patient appeared hypo-functional, while the total brain volume was increased, thus contrasting, in an opposite and intriguing manner, with the global brain volume reduction reported in WBS. Even if these findings come from the analysis of a single patient and, therefore, have to be considered preliminary results, they encourage carrying on further functional and volumetric studies in patients with 7q11.23 duplication, to fully elucidate the role of this gene-dosage alteration on brain development and limbic system function.

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Year:  2014        PMID: 24722762     DOI: 10.1007/s10803-014-2117-7

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


  17 in total

Review 1.  Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.

Authors:  Andreas Meyer-Lindenberg; Carolyn B Mervis; Karen Faith Berman
Journal:  Nat Rev Neurosci       Date:  2006-05       Impact factor: 34.870

2.  MRI amygdala volume in Williams Syndrome.

Authors:  Liliana Capitão; Adriana Sampaio; Cassandra Sampaio; Cristiana Vasconcelos; Montse Férnandez; Elena Garayzábal; Martha E Shenton; Oscar F Gonçalves
Journal:  Res Dev Disabil       Date:  2011-07-12

3.  Aicardi syndrome associated with autosomal genomic imbalance: coincidence or evidence for autosomal inheritance with sex-limited expression?

Authors:  P Prontera; A Bartocci; V Ottaviani; I Isidori; D Rogaia; C Ardisia; G Guercini; A Mencarelli; E Donti
Journal:  Mol Syndromol       Date:  2013-04-11

Review 4.  Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Authors:  Giuseppe Merla; Nicola Brunetti-Pierri; Lucia Micale; Carmela Fusco
Journal:  Hum Genet       Date:  2010-05-01       Impact factor: 4.132

5.  Rare de novo and transmitted copy-number variation in autistic spectrum disorders.

Authors:  Dan Levy; Michael Ronemus; Boris Yamrom; Yoon-ha Lee; Anthony Leotta; Jude Kendall; Steven Marks; B Lakshmi; Deepa Pai; Kenny Ye; Andreas Buja; Abba Krieger; Seungtai Yoon; Jennifer Troge; Linda Rodgers; Ivan Iossifov; Michael Wigler
Journal:  Neuron       Date:  2011-06-09       Impact factor: 17.173

6.  Functional magnetic resonance imaging of facial information processing in children with autistic disorder, attention deficit hyperactivity disorder and typically developing controls.

Authors:  Krisztina L Malisza; Christine Clancy; Deborah Shiloff; Jeanette Holden; Cheryl Jones; Kristjan Paulson; Dickie C T Yu; Randy Summers; Albert E Chudley
Journal:  Int J Adolesc Med Health       Date:  2011

Review 7.  The nature of brain dysfunction in autism: functional brain imaging studies.

Authors:  Nancy J Minshew; Timothy A Keller
Journal:  Curr Opin Neurol       Date:  2010-04       Impact factor: 5.710

8.  Amygdala volume in adults with posttraumatic stress disorder: a meta-analysis.

Authors:  Fu L Woon; Dawson W Hedges
Journal:  J Neuropsychiatry Clin Neurosci       Date:  2009       Impact factor: 2.198

9.  Brain size and brain/intracranial volume ratio in major mental illness.

Authors:  Martin Reite; Erik Reite; Dan Collins; Peter Teale; Donald C Rojas; Elliot Sandberg
Journal:  BMC Psychiatry       Date:  2010-10-11       Impact factor: 3.630

10.  Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus.

Authors:  Claudia Torniero; Bernardo dalla Bernardina; Francesca Novara; Annalisa Vetro; Ivana Ricca; Francesca Darra; Tiziano Pramparo; Renzo Guerrini; Orsetta Zuffardi
Journal:  Eur J Hum Genet       Date:  2006-10-31       Impact factor: 4.246

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  7 in total

1.  Children with 7q11.23 duplication syndrome: psychological characteristics.

Authors:  Carolyn B Mervis; Bonita P Klein-Tasman; Myra J Huffman; Shelley L Velleman; C Holley Pitts; Danielle R Henderson; Janet Woodruff-Borden; Colleen A Morris; Lucy R Osborne
Journal:  Am J Med Genet A       Date:  2015-04-21       Impact factor: 2.802

2.  7q11.23 Duplication syndrome: Physical characteristics and natural history.

Authors:  Colleen A Morris; Carolyn B Mervis; Alex P Paciorkowski; Omar Abdul-Rahman; Sarah L Dugan; Alan F Rope; Patricia Bader; Laura G Hendon; Shelley L Velleman; Bonita P Klein-Tasman; Lucy R Osborne
Journal:  Am J Med Genet A       Date:  2015-09-03       Impact factor: 2.802

Review 3.  The 7q11.23 Microduplication Syndrome: A Clinical Report with Review of Literature.

Authors:  Elham Abbas; Devin M Cox; Teri Smith; Merlin G Butler
Journal:  J Pediatr Genet       Date:  2016-06-15

4.  7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling.

Authors:  Maria Lisa Dentici; Paola Bergonzini; Francesco Scibelli; Cristina Caciolo; Paola De Rose; Francesca Cumbo; Viola Alesi; Rossella Capolino; Ginevra Zanni; Lorenzo Sinibaldi; Antonio Novelli; Marco Tartaglia; Maria Cristina Digilio; Bruno Dallapiccola; Stefano Vicari; Paolo Alfieri
Journal:  Brain Sci       Date:  2020-11-11

Review 5.  Genetic and Epigenetic Etiology Underlying Autism Spectrum Disorder.

Authors:  Sang Hoon Yoon; Joonhyuk Choi; Won Ji Lee; Jeong Tae Do
Journal:  J Clin Med       Date:  2020-03-31       Impact factor: 4.241

6.  Copy number variations associated with fetal congenital kidney malformations.

Authors:  Meiying Cai; Na Lin; Linjuan Su; Xiaoqing Wu; Xiaorui Xie; Ying Li; Xuemei Chen; Yuan Lin; Hailong Huang; Liangpu Xu
Journal:  Mol Cytogenet       Date:  2020-03-24       Impact factor: 2.009

7.  Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.

Authors:  Meiying Cai; Na Lin; Linjuan Su; Xiaoqing Wu; Xiaorui Xie; Ying Li; Xuemei Chen; Yifang Dai; Yuan Lin; Hailong Huang; Liangpu Xu
Journal:  J Clin Lab Anal       Date:  2019-09-10       Impact factor: 2.352

  7 in total

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