| Literature DB >> 22855654 |
T I Mancini1, M M Oliveira, A R N Dutra, A B A Perez, R M Minillo, S S Takeno, M I Melaragno.
Abstract
We present a 2-year-old boy with a de novo 46,XY,idic(Y)(q11.221),del(4)(q26q31.1) karyotype. G-banding, FISH, MLPA, and SNP-array techniques were used to characterize the 24-Mb deletion in 4q and the breakpoint in the isodicentric Y-chromosome region between 15,982,252 and 15,989,842 bp. The patient presented with mild facial dysmorphism, hemangioma, mild frontal cerebral atrophy, and Dandy-Walker variant. Essentially, this case reveals that patients can present more complex genomic imbalances than initially suspected.Entities:
Year: 2012 PMID: 22855654 PMCID: PMC3398833 DOI: 10.1159/000338468
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769