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家长报告的 13 三体综合征成人病史。

Parent-reported histories of adults with trisomy 13 syndrome.

机构信息

Division of Medical Genetics, Department of Pediatrics, University of Utah Health, Salt Lake City, Utah, USA.

出版信息

Am J Med Genet A. 2021 Jun;185(6):1743-1756. doi: 10.1002/ajmg.a.62165. Epub 2021 Mar 22.

Abstract

Clinical histories and outcome data of long-term survivors with trisomy 13 are rare. The goal of this study was to collect the medical histories of adult individuals (≥18 years old) with apparent non-mosaic trisomy 13/Patau syndrome to help gain further insight in to the clinical course for individuals with this condition and to characterize the manifestations for surveillance and management. We collected 11 families through a contact person with the LWT13 (Living with Trisomy 13) LIFE support group. We performed telephone interviews to gather their medical histories and report these data in system-based summaries, tables, and clinical vignettes. In instances where parents retained copies of genetic testing reports or clinicians currently taking care of the individual with trisomy 13 were able to provide documentation, we confirmed diagnosis. All clinical histories and reported manifestations were consistent with a diagnosis of trisomy 13. We also elicited comments from parents on their personal experiences of raising an individual with trisomy 13.

摘要

患有三体 13 综合征(即 13 号染色体三体)的长期存活者的临床病史和结局数据较为罕见。本研究旨在收集成年个体(≥18 岁)的明显非嵌合性三体 13/帕陶综合征的医学病史,以帮助进一步了解此类患者的临床病程,并确定用于监测和管理的表现特征。我们通过 LWT13(三体 13 生存)LIFE 支持小组的联系人收集了 11 个家庭的信息。我们通过电话访谈收集了他们的医学病史,并以系统为基础的摘要、表格和临床病例报告的形式呈现这些数据。在父母保留了基因检测报告副本的情况下,或者当前照顾三体 13 患者的临床医生能够提供相关文件,我们就可以确认诊断。所有的临床病史和报告的表现都与三体 13 综合征的诊断相符。我们还征求了家长对于养育三体 13 综合征患者的个人经验的意见。

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