BIOGENET, Medical and Forensic Genetics Laboratory, Cosenza, Italy.
Department of Biology, Ecology and Earth Sciences, University of Calabria, Rende, Italy.
Mol Genet Genomic Med. 2023 Apr;11(4):e2130. doi: 10.1002/mgg3.2130. Epub 2023 Jan 24.
The 3q29 microduplication syndrome is a rare genomic disorder characterized by an extremely variable neurodevelopmental phenotype usually involving a genomic region ranging from 1.6 to 1.76 Mb. A small microduplication of 448.8 Kb containing only two genes was recently described in a patient with a 3q29 microduplication that was proposed as the minimal critical region of overlap of this syndrome.
Molecular karyotyping (array-CGH) was performed on DNA extracted from peripheral blood samples using Agilent-California USA Human Genome CGH Microarray 4 × 180 K. The proband and his younger brother were further tested with a next generation sequencing (NGS) panel including genes implicated in autism spectrum disorder and in neurodevelopmental disorders. Quantitative real-time PCR was applied to verify the abnormal array-CGH findings.
Here, we report on a family with two males with neurodevelopmental disorders and an unaffected sibling with a small 3q29 microduplication (432.8 Kb) inherited from an unaffected mother that involves only two genes: DGL1 and BDH1. The proband had an additional intragenic duplication inherited from the unaffected father. Further testing was negative for Fragile X syndrome and for genes implicated in autism spectrum disorder and in neurodevelopmental disorders.
To the best of our knowledge, one of the family members here analyzed is the second reported case of a patient carrying a small 3q29 microduplication including only DGL1 and BDH1 genes and without any additional genetic aberration. The recognition of the clinical spectrum in patients with the critical region of overlap associated with the 3q29 duplication syndrome should prove valuable for predicting outcomes and providing more informed genetic counseling to patients with duplications in this region.
3q29 微重复综合征是一种罕见的基因组疾病,其神经发育表型变化极大,通常涉及 1.6 至 1.76 Mb 的基因组区域。最近在一名患有 3q29 微重复的患者中描述了一个 448.8 Kb 的小微重复,其中仅包含两个基因,该重复被提议为该综合征重叠的最小关键区域。
使用 Agilent-California USA Human Genome CGH Microarray 4 × 180 K 对来自外周血样本的 DNA 进行分子核型分析(array-CGH)。对先证者及其弟弟进行了进一步的下一代测序(NGS)面板检测,该面板包括自闭症谱系障碍和神经发育障碍相关基因。应用实时定量 PCR 验证异常 array-CGH 结果。
在这里,我们报告了一个家庭,其中两名男性患有神经发育障碍,一名未受影响的兄弟姐妹从未受影响的母亲那里遗传了一个小的 3q29 微重复(432.8 Kb),仅涉及两个基因:DGL1 和 BDH1。先证者从未受影响的父亲那里继承了一个额外的基因内重复。脆性 X 综合征及自闭症谱系障碍和神经发育障碍相关基因检测均为阴性。
据我们所知,在此分析的家庭成员之一是第二个报告的仅携带 DGL1 和 BDH1 基因且无任何其他遗传异常的小 3q29 微重复患者。与 3q29 重复综合征相关的关键区域重叠患者的临床谱的识别,应该有助于预测结果并为该区域重复的患者提供更具信息性的遗传咨询。