| Literature DB >> 31602194 |
Lélia L Gonçalves Ramos1,2, Irene Plaza Pinto2,3, Rajib Deb2,4, Cristiano L Ribeiro2,3, Damiana Mírian da Cruz E Cunha2, Lysa Bernardes Minasi2,5, Antonio M T Cordeiro Silva1,6, Aparecido D da Cruz2,3,5,7.
Abstract
We report the case of a child from Central Brazil with global developmental delay (GDD), syndromic features, and absence of abnormal skin pigmentation, nail dystrophy, and leukoplakia of the oral mucosa, with a rearrangement at Xq28 harboring the DKC1 gene. GTC-banding revealed a male karyotype (46,XY) with no visible numerical or structural alterations. Chromosomal microarray analysis (CMA) showed a 0.36-Mb gain at Xq28 of maternal origin, encompassing 22 genes, including DKC1. Rearrangements and mutations involving this gene have been associated with dyskeratosis congenita, X-linked (OMIM 305000) and Hoyeraal-Hreidarsson syndrome. CMA was a powerful and efficient approach to identify a gain at Xq28 harboring the DKC1 gene in our patient with GDD syndromic features and no cutaneous alterations, suggesting that this variant is associated with the Hoyeraal-Hreidarsson syndrome.Entities:
Keywords: Chromosomal microarray analysis; DKC1; Genetic syndrome; Global developmental delay
Year: 2019 PMID: 31602194 PMCID: PMC6738202 DOI: 10.1159/000500005
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769