Kósa Magdolna, Horváth Emese, Kalmár Tibor, Maróti Zoltán, Földesi Imre, Bereczki Csaba
Department of Pediatrics and Pediatric Health Center, Albert Szent-Györgyi Health Centre, University of Szeged, Szeged, Hungary.
Department of Medical Genetics, Albert Szent-Györgyi Health Centre, University of Szeged, Szeged, Hungary.
J Pediatr Genet. 2022 Dec 1;13(4):320-325. doi: 10.1055/s-0042-1757621. eCollection 2024 Dec.
Although data on T18 are widespread, there is a lack of knowledge on mosaic trisomy 18 (mT18). A current review of mT18 symptomatology, long-term follow-up, and potential health risks is lacking for health care professionals. Our paper addresses these, emphasizing the importance of regular tumor screening as a key message for mT18 patient follow-up. We also present the case of a female patient with mT18 who presented with diaphragmatic relaxation and cyclic vomiting syndrome (CVS), which had previously not been reported in this genetic condition. On further investigating the etiology of CVS, we revealed a novel mitochondrial mutation in the gene in heteroplasmic form. Based on the literature, we hypothesize that the mitochondrial mutation together with mT18 could result in CVS.
尽管关于18三体综合征(T18)的数据很普遍,但对于嵌合型18三体综合征(mT18)却缺乏了解。目前缺乏针对医疗保健专业人员的mT18症状学、长期随访及潜在健康风险的综述。我们的论文阐述了这些内容,强调定期肿瘤筛查作为mT18患者随访关键信息的重要性。我们还报告了一例患有mT18的女性患者,该患者出现膈肌松弛和周期性呕吐综合征(CVS),而此前在这种遗传疾病中尚未有过此类报道。在进一步研究CVS的病因时,我们发现了该基因中一种新的异质性线粒体突变。基于文献,我们推测线粒体突变与mT18共同作用可能导致CVS。