The First Korean Case Report of Siblings with 12q24.22q24.33 Duplication
- Author:
Se Hwan MOON
1
;
Jung-Sook HA
;
Jun chul BYUN
;
Hee Joung CHOI
;
So Yun PARK
Author Information
- Publication Type:Case Report
- From:Keimyung Medical Journal 2024;43(1):54-58
- CountryRepublic of Korea
- Language:EN
- Abstract: Live-born cases of partial trisomy 12q are rare, and only a few fetuses with this unbalanced translocation have survived to term. To our knowledge, only about 40 patients have been reported as having 12q duplication, and among them are no Korean reports. Here, we report the first Korean case of siblings with a 12q24.22q24.33 duplication. An 11-year-old boy visited our clinic for short stature. He was born small for his gestational age and had distinctive facial features, a history of surgery for anorectal malformation, psychomotor delay, intellectual disabilities, and attention-deficit/hyperactivity disorder (ADHD). He had an older sister with similar clinical features. The chromosomal microarray of the patient and his sister showed identical results: a 16.2 Mb duplication of 12q24.22q24.33. They had an identical cutoff point, but their symptoms were not. Symptoms common to both included growth retardation, psychomotor delay, intellectual disability, ADHD, and small for their gestational age.
