Keimyung Med J.  2024 Jun;43(1):54-58. 10.46308/kmj.2023.00192.

The First Korean Case Report of Siblings with 12q24.22q24.33 Duplication

• Moon SH
• Ha JS
• Byun Jc
• Choi HJ
• Park SY

• KMID: 2556372
• DOI: http://doi.org/10.46308/kmj.2023.00192

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.

Keyword

Attention deficit disorder with hyperactivity; Fetal growth retardation; Intellectual disability; Microarray analysis; Trisomy 12q