Literature DB >> 23524024

A parallel study of different array-CGH platforms in a set of Spanish patients with developmental delay and intellectual disability.

Laia Rodríguez-Revenga1, Elena Vallespín, Irene Madrigal, María Palomares, Antonio Mur, Sixto García-Miñaur, Fernando Santos, M Ángeles Mori, Pablo Lapunzina, Montserrat Mila, Julián Nevado.   

Abstract

Developmental delay and intellectual disability, which occur in 1-3% of the population, account for a large number of the cases regularly seen in genetic units. Chromosomal microarray analysis has been shown to be a valuable clinical diagnostic assay and it should be the first-tier clinical diagnostic test for individuals with these conditions. However and due to several difficulties such as the platform resolution, the cost, and the inexperience with genomic data bases, the implementation of this test in many cytogenetic laboratories has been delayed. In an attempt to provide more insights of the benefits derived by using the chromosomal microarray analysis, this study presents the experience of two clinical centers using three different microarray platforms. The results obtained using a custom microarray (KaryoArray®) and two different commercial medium- and high-resolution whole-genome oligonucleotide microarrays have been compared. An overall diagnostic yield of around 15% has been obtained. However, the custom microarray platform has been shown to be more convenient for a clinical setting, since it allows the detection of more pathogenic copy number variants and less common variants.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23524024     DOI: 10.1016/j.gene.2013.02.043

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  6 in total

1.  Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.

Authors:  Lucía Daniela Espeche; Andrea Paula Solari; María Ángeles Mori; Rubén Martín Arenas; María Palomares; Myriam Pérez; Cinthia Martínez; Vanesa Lotersztein; Mabel Segovia; Romina Armando; Liliana Beatriz Dain; Julián Nevado; Pablo Lapunzina; Sandra Rozental
Journal:  Mol Biol Rep       Date:  2020-09-13       Impact factor: 2.316

2.  Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability.

Authors:  Diana Miclea; Adriana Szucs; Andreea Mirea; Delia-Maria Stefan; Florina Nazarie; Simona Bucerzan; Cecilia Lazea; Alina Grama; Tudor Lucian Pop; Marius Farcas; Gabriela Zaharie; Melinda Matyas; Monica Mager; Mihaela Vintan; Radu Popp; Camelia Alkhzouz
Journal:  Int J Gen Med       Date:  2021-08-16

3.  Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients.

Authors:  Nancy Choucair; Joelle Abou Ghoch; Sandra Corbani; Pierre Cacciagli; Cecile Mignon-Ravix; Nabiha Salem; Nadine Jalkh; Sandra El Sabbagh; Ali Fawaz; Tony Ibrahim; Laurent Villard; André Mégarbané; Eliane Chouery
Journal:  Mol Cytogenet       Date:  2015-04-09       Impact factor: 2.009

4.  Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patients.

Authors:  Isabel Marques Carreira; Susana Isabel Ferreira; Eunice Matoso; Luís Miguel Pires; José Ferrão; Ana Jardim; Alexandra Mascarenhas; Marta Pinto; Nuno Lavoura; Cláudia Pais; Patrícia Paiva; Lúcia Simões; Francisco Caramelo; Lina Ramos; Margarida Venâncio; Fabiana Ramos; Ana Beleza; Joaquim Sá; Jorge Saraiva; Joana Barbosa de Melo
Journal:  Mol Cytogenet       Date:  2015-12-30       Impact factor: 2.009

5.  Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohort.

Authors:  Wilson Wai Sing Chong; Ivan Fai Man Lo; Stephen Tak Sum Lam; Chi Chiu Wang; Ho Ming Luk; Tak Yeung Leung; Kwong Wai Choy
Journal:  Mol Cytogenet       Date:  2014-05-23       Impact factor: 2.009

6.  The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.

Authors:  Sarah M Al-Qattan; Salma M Wakil; Shamsa Anazi; Anas M Alazami; Nisha Patel; Ranad Shaheen; Hanan E Shamseldin; Samya T Hagos; Haya M AlDossari; Mustafa A Salih; Heba Y El Khashab; Amal Y Kentab; Mohammed N AlNasser; Fahad A Bashiri; Namik Kaya; Mais O Hashem; Fowzan S Alkuraya
Journal:  Genet Med       Date:  2014-12-11       Impact factor: 8.822

  6 in total

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