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 shortterm 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 genedosage alteration on brain development and limbic system function.

Brief report: Functional MRI of a patient with 7q11.23 duplication syndrome and autism spectrum disorder / P. Prontera, D. Serino, B. Caldini, L. Scarponi, G. Merla, G. Testa, M. Muti, V. Napolioni, G. Mazzotta, M. Piccirilli, E. Donti. - In: JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS. - ISSN 0162-3257. - 44:10(2014), pp. 2608-2613.

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

G. Testa;
2014

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 shortterm 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 genedosage alteration on brain development and limbic system function.
7q11.23 Duplication; Amygdala; Autism spectrum disorders; Functional magnetic resonance; Limbic system; Magnetic resonance; Williams–Beuren syndrome; Adolescent; Child; Child Development Disorders, Pervasive; Female; Humans; Limbic System; Male; Research Report; Williams Syndrome; Young Adult; Magnetic Resonance Imaging; Developmental and Educational Psychology; Medicine (all)
Settore MED/39 - Neuropsichiatria Infantile
Settore MED/03 - Genetica Medica
Settore MED/36 - Diagnostica per Immagini e Radioterapia
2014
Article (author)
File in questo prodotto:
File Dimensione Formato  
Prontera et al. JADD 2014.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 2.57 MB
Formato Adobe PDF
2.57 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/354272
Citazioni
  • ???jsp.display-item.citation.pmc??? 8
  • Scopus 13
  • ???jsp.display-item.citation.isi??? 13
social impact