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Updated: Mar 25, 2026

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
Published on: February 21, 2015
[Chromosome 7q11.23 duplication syndrome. First reported case in Latin America]
Felipe Ruiz Botero1, Wilmar Saldarriaga Gil2,3, Carolina Isaza de Lourido2,3
1Centro de Investigación en Anomalías Congénitas y Enfermedades Raras (CIACER), Facultad de Ciencias de la Salud, Universidad Icesi, Cali, Colombia. Fruiz@icesi.edu.co.
Abstract:
7q11.23 duplication syndrome is a disease caused by duplication of a region of chromosome 7 comprising 26 genes. The first case described in the literature was reported by Somerville et al. in 2005, who described a patient with dolichocephaly, high and narrow forehead, long eyelashes, high and wide nose, short philtrum, high arched palate, dental malocclusion, retrognathia, and severe language delay. We report the case of a Colombian patient with 7q11.23 duplication by comparative genomic hybridization techniques, and classical clinical findings, this being the first reported case in Colombia and Latin America.
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