Tang Dan, Chen Ai, Xu Jing, Huang Yu, Fan Jun, Wang Jin, Zhu Hui, Pi Guanghuan, Yang Li, Xiong Fu, Luo Zemin, Li Gen, Zeng Lan, Zhu Shuyao
Department of Pediatrics, Sichuan Provincial Woman's and Children's Hospital, The Affiliated Women's and Children's Hospital of Chengdu Medical College, Chengdu, China.
Department of Pediatrics, The Second People's Hospital of Chengdu City, Chengdu, China.
BMC Med Genomics. 2024 Dec 23;17(1):294. doi: 10.1186/s12920-024-02059-3.
Pure partial trisomy 16q12.1q22.1 is a rare chromosome copy number variant (CNV). The primary clinical phenotypes associated with this syndrome include abnormal facial morphology, global developmental delay (GDD), short stature, and reported predisposing factors for atypical behavior, autism, the development of learning disabilities, and neuropsychiatric disorders. The dosage-sensitive genes associated with partial trisomy are not disclosed preventing to establish a genotype-phenotype correlation.
We report a case of a Chinese patient diagnosed with GDD and an abnormal facial shape, who was found to have partial trisomy 16 through karyotyping and high-throughput sequencing analysis. Karyotype and CNV tracing analyses were also conducted on the biological parents of the patient to assess for any chromosomal structural abnormalities. Additionally, we included 29 patients with pure partial trisomy 16q, reported in the DECIPHER database and the literature. We and performed a genotype-phenotype correlation analysis.
The proband, a 2-year-old female, was found to have a de novo 21.96 Mb duplication located between 16q12.1q22.1, with no other deletions observed on other chromosomes, indicating a pure partial trisomy of 16q. Through genotype and phenotype analysis of 29 individuals, we found that patients with the duplicated region located at the distal region of 16q may exhibit more severe symptoms than those with duplication at the proximal region; however, no relationship was identified between phenotype and the size of the duplicated segment.
We report, for the first time, a patient with partial trisomy 16q validated by multiple genetic tests, including CNV-seq, whole exome sequencing (WES), and karyotyping. It is speculated that partial trisomy of 16q may be associated with continuous gene duplication. However, functional studies are necessary to identify the causative gene or critical region linked to duplication syndrome of chromosome 16q.
纯合16q12.1q22.1部分三体是一种罕见的染色体拷贝数变异(CNV)。与该综合征相关的主要临床表型包括面部形态异常、全面发育迟缓(GDD)、身材矮小,以及报道的非典型行为、自闭症、学习障碍和神经精神疾病的易感因素。与部分三体相关的剂量敏感基因尚未公开,这妨碍了建立基因型与表型的相关性。
我们报告了一例被诊断为GDD且面部形状异常的中国患者,通过核型分析和高通量测序分析发现其患有16号染色体部分三体。还对患者的生物学父母进行了核型和CNV追踪分析,以评估是否存在任何染色体结构异常。此外,我们纳入了DECIPHER数据库和文献中报道的29例纯合16q部分三体患者。我们进行了基因型与表型的相关性分析。
先证者为一名2岁女性,发现其16q12.1q22.1之间存在一个21.96 Mb 的新发重复,其他染色体未观察到其他缺失,表明为16q纯合部分三体。通过对29例个体的基因型和表型分析,我们发现重复区域位于16q远端的患者可能比近端重复者表现出更严重的症状;然而,未发现表型与重复片段大小之间的关系。
我们首次报告了一例经多种基因检测(包括CNV测序、全外显子测序(WES)和核型分析)验证的16q部分三体患者。推测16q部分三体可能与连续基因重复有关。然而,需要进行功能研究以确定与16q染色体重复综合征相关的致病基因或关键区域。