Health Research Institute of the Balearic Islands (IdISBa), Genomics of Health research group, Palma, Spain.
Hospital Universitari Son Espases, Unit of Molecular Diagnostics and Clinical Genetics, Palma, Spain.
Am J Med Genet A. 2024 Dec;194(12):e63830. doi: 10.1002/ajmg.a.63830. Epub 2024 Aug 2.
Tuberous sclerosis complex (TSC) and autosomal dominant polycystic kidney disease (ADPKD) are genetically distinct disorders typically associated with pathogenic variants in TSC1 and TSC2 for the former and PKD1 and PKD2 for the latter. TSC2 and PKD1 lie adjacent to each other, and large deletions comprising both genes lead to TSC2/PKD1 contiguous gene deletion syndrome (CGS). In this study, we describe a young female patient exhibiting symptoms of TSC2/PKD1 CGS in which genetic analysis disclosed two noncontiguous partial gene deletions in TSC2 and PKD1 that putatively are responsible for the manifestations of the syndrome. Further analysis revealed that both deletions appear to be de novo on the maternal chromosome, presumably with a germline origin. Despite extensive analysis, no maternal chromosomal rearrangement triggering these pathogenic variants was detected. This case elucidates a unique pathogenesis for TSC2/PKD1 CGS, diverging from the common contiguous deletions typically observed, marking the first reported instance of TSC2/PKD1 CGS caused by independent, functionally significant partial gene deletions.
结节性硬化症复合征(TSC)和常染色体显性多囊肾病(ADPKD)是两种遗传上不同的疾病,前者通常与 TSC1 和 TSC2 的致病变异相关,后者则与 PKD1 和 PKD2 相关。TSC2 和 PKD1 彼此相邻,包含这两个基因的大片段缺失导致 TSC2/PKD1 连续基因缺失综合征(CGS)。在本研究中,我们描述了一位年轻女性患者,其表现出 TSC2/PKD1 CGS 的症状,基因分析显示 TSC2 和 PKD1 中存在两个非连续的部分基因缺失,推测这些缺失与该综合征的表现有关。进一步分析表明,这两个缺失似乎均来自于母源染色体,可能具有种系起源。尽管进行了广泛的分析,但未检测到导致这些致病性变异的母源染色体重排。该病例阐明了 TSC2/PKD1 CGS 的独特发病机制,与常见的连续缺失不同,标志着首例由独立、具有功能意义的部分基因缺失引起的 TSC2/PKD1 CGS 病例。