New microdeletion and microduplication syndromes: A comprehensive review

86Citations
Citations of this article
136Readers
Mendeley users who have this article in their library.

Abstract

Several new microdeletion and microduplication syndromes are emerging as disorders that have been proven to cause multisystem pathologies frequently associated with intellectual disability (ID), multiple congenital anomalies (MCA), autistic spectrum disorders (ASD) and other phenotypic findings. In this paper, we review the "new" and emergent microdeletion and microduplication syndromes that have been described and recognized in recent years with the aim of summarizing their main characteristics and chromosomal regions involved. We decided to group them by genomic region and within these groupings have classified them into those that include ID, MCA, ASD or other findings. This review does not intend to be exhaustive but is rather a quick guide to help pediatricians, clinical geneticists, cytogeneticists and/or molecular geneticists. © 2014, Sociedade Brasileira de Genética. Printed in Brazil.

Cite

CITATION STYLE

APA

Nevado, J., Mergener, R., Palomares-Bralo, M., Souza, K. R., Vallespín, E., Mena, R., … Lapunzina, A. P. (2014). New microdeletion and microduplication syndromes: A comprehensive review. Genetics and Molecular Biology. Brazilian Journal of Genetics. https://doi.org/10.1590/S1415-47572014000200007

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free