A Rare de novo Interstitial Duplication at 4p15.2 in a Boy with Severe Congenital Heart Defects, Limb Anomalies, Hypogonadism, and Global Developmental Delay

• Published in: Cytogenetic and genome research Vol. 150; no. 2; p. 112
• Main Authors: Liang, Liyang, Xie, Yingjun, Shen, Yiping, Yin, Qibin, Yuan, Haiming
• Format: Journal Article
• Language: English
• Published: Switzerland 01.01.2016
• Subjects: Abnormalities, Multiple - genetics; Abnormalities, Multiple - pathology; Child, Preschool; Chromosome Disorders - genetics; Chromosome Disorders - pathology; Chromosomes, Human, Pair 4 - genetics; Developmental Disabilities - genetics; Heart Defects, Congenital - genetics; Humans; Hypogonadism - genetics; Limb Deformities, Congenital - genetics; Male; Trisomy - genetics; Trisomy - pathology
• ISSN: 1424-859X
• DOI: 10.1159/000454698

Proximal 4p deletion syndrome is a relatively rare genetic condition characterized by dysmorphic facial features, limb anomalies, minor congenital heart defects, hypogonadism, cafe-au-lait spots, developmental delay, tall and thin habitus, and intellectual disability. At present, over 20 cases of this syndrome have been published. However, duplication of the same region in proximal 4p has never been reported. Here, we describe a 2-year-5-month-old boy with severe congenital heart defects, limb anomalies, hypogonadism, distinctive facial features, pre- and postnatal developmental delay, and mild cognitive impairments. A de novo 4.5-Mb interstitial duplication at 4p15.2p15.1 was detected by chromosomal microarray analysis. Next-generation sequencing was employed and confirmed the duplication, but revealed no additional pathogenic variants. Several candidate genes in this interval responsible for the complex clinical phenotype were identified, such as RBPJ, STIM2, CCKAR, and LGI2. The results suggest a novel contiguous gene duplication syndrome.