P491: Mosaic double aneuploidy: A rare case of 45,X/47,XX,+18 mosaicism and review of the literature
folds, broad flat nasal tip, hypotonia, dental crowding, and flat feet.Medical complications include dextroscoliosis, hypotonia, osteoporosis, and astigmatism.At 14-years-old, height is 1.435m (< 1st percentile), although head circumference is 54.5 cm and weight is 61.2 kg, both within normal ranges.Diagnostic Workup: Karyotype analysis revealed 46,XX,dup(1)(q42q44). SNV microarray revealed microarray revealed a 19.24 Mb duplication of 1q32.2q42.13.Chromosomal analysis on both parents was normal, suggesting this variant was de novo or a result of gonadal mosaicism.Brain MRI revealed hypoplastic corpus callosum and hippocampus and an abnormal cingulate gyrus.
Authors
- Teresa Campbell
- Cate Paschal (ORCID: https://orcid.org/0000-0002-9400-5560)
- Candace T. Myers (ORCID: https://orcid.org/0000-0002-7047-2754)
- Alexandra Keefe (ORCID: https://orcid.org/0009-0009-2455-1687)
Institutions
- Seattle Children's Hospital (US)
Publication Details
- Journal
- Genetics in Medicine Open
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1016/j.gimo.2025.103358
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00