| Literature DB >> 36267867 |
Amal Alhashem1,2, Saria Alazmeh1, Ayla Barakat1, Ahmed Alfares2,3, Hatem Elghezal4.
Abstract
Ring chromosome 15 is a rare chromosomal disorder, which usually occurs during early embryonic development via spontaneous errors and has variable presentation. To date, 89 cases of this condition have been reported. This case report describes a 5-year-old Saudi boy who was diagnosed as having de novo 46,XY,r(15). The patient presented with short stature, speech delay, café au lait spots, and facial dysmorphic features, together with new findings of left crossed fused renal ectopia and 11 ribs. This presentation was compared with the findings of cases reported previously. Thieme. All rights reserved.Entities:
Keywords: array CGH; ring chromosome 15; short stature
Year: 2020 PMID: 36267867 PMCID: PMC9578776 DOI: 10.1055/s-0040-1721135
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X