| Literature DB >> 29441220 |
Jess F Peterson1, Gabrielle C Geddes2, Donald G Basel2,3, Dana Schippman2, John W Grignon4, Peter vanTuinen1, Ulrike P Kappes3,5.
Abstract
We report a 4-month-old male proband with a history of prominent forehead, hypertelorism, ear abnormalities, micrognathia, hypospadias, and multiple cardiac abnormalities. Initial microarray analysis detected a concurrent 7p21.3-p22.3 duplication and 13q33.2-q34 deletion indicating an unbalanced rearrangement. However, subsequent conventional cytogenetic studies only revealed what appeared to be a balanced t(12;20)(q24.33;p12.2). Fluorescence in situ hybridization (FISH) using chromosome-specific subtelomere probes confirmed the presence of an unbalanced der(13)t(7;13)(p21.3;q33.2) and balanced t(12;20)(q24.33;p12.2), both of maternal origin. In addition to our unique clinical findings, this case highlights the benefits and limitations of both conventional cytogenetic studies and microarray analysis and how FISH complements each methodology.Entities:
Keywords: 13q33.2-q34 deletion; 7p21.3-p22.3 duplication; array comparative genomic hybridization; double balanced translocation carrier; fluorescence in situ hybridization; unbalanced translocation
Year: 2017 PMID: 29441220 PMCID: PMC5809171 DOI: 10.1055/s-0037-1605592
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X