A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism

Title
A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism
Authors
김창렬
Keywords
1q duplication; 18q deletion; Array comparative genomic hybridization; Developmental delay; Dysmorphism
Issue Date
2016-02
Publisher
대한소아과학회
Citation
Korean Journal of Pediatrics, v. 59, NO 2, Page. 91-95
Abstract
We report the case of a 22-month-old boy with a new mosaic partial unbalanced translocation of 1q and 18q. The patient was referred to our Pediatric Department for developmental delay. He showed mild facial dysmorphism, physical growth retardation, a hearing disability, and had a history of patent ductus arteriosus. White matter abnormality on brain magnetic resonance images was also noted. His initial routine chromosomal analysis revealed a normal 46,XY karyotype. In a microarray-based comparative genomic hybridization (aCGH) analysis, subtle copy number changes in 1q32.1–q44 (copy gain) and 18q21.33–18q23 (copy loss) suggested an unbalanced translocation of t(1;18). Repeated chromosomal analysis revealed a low-level mosaic translocation karyotype of 46,XY,der(18)t(1;18)(q32.1;q21.3)[12]/46,XY[152]. Because his parents had normal karyotypes, his translocation was considered to be de novo. The abnormalities observed in aCGH were confirmed by metaphase fluorescent in situ hybridization. We report this patient as a new karyotype presenting developmental delay, facial dysmorphism, cerebral dysmyelination, and other abnormalities.
URI
https://synapse.koreamed.org/DOIx.php?id=10.3345/kjp.2016.59.2.91http://hdl.handle.net/20.500.11754/33999
ISSN
1738-1061; 2092-7258
DOI
http://dx.doi.org/10.3345/kjp.2016.59.2.91
Appears in Collections:
COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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