Department of Genomic Medicine and Pediatric Genetics, Vanderbilt University Medical Center, Nashville, Tennessee.
Clinical Cancer Genetics Services, Weill Cornell Medicine, New York, New York.
J Genet Couns. 2020 Dec;29(6):1151-1158. doi: 10.1002/jgc4.1275. Epub 2020 Mar 20.
Neurofibromatosis type 1 (NF1) is a genetic condition characterized by various cutaneous, neurological and psychological manifestations. The present study examined whether parental knowledge of NF1 is associated with a parent's NF1 status, affected or unaffected, and exposure to genetic counseling. Parents of children with NF1 were invited to complete an online survey answering true or false and multiple-choice questions to evaluate their overall knowledge of NF1. The study included 274 respondents, of which NF1 knowledge scores were significantly higher for unaffected parents (p < .001), and for parents who reported previously meeting with a genetic counselor (p < .001). Items pertaining to NF1-related cancer were least likely to be answered correctly. The results of the current study revealed lower overall NF1 knowledge in affected parents and knowledge gaps identifying areas where focused NF1 education may be beneficial.
神经纤维瘤病 1 型(NF1)是一种遗传疾病,其特征为各种皮肤、神经和心理表现。本研究旨在探讨父母对 NF1 的了解是否与父母的 NF1 状况(受影响或未受影响)以及是否接受过遗传咨询有关。研究邀请了 NF1 患儿的父母完成一项在线调查,回答是/否和多项选择题,以评估他们对 NF1 的总体了解。该研究共纳入 274 名受访者,结果显示,未受影响父母的 NF1 知识得分显著更高(p<0.001),而报告曾与遗传咨询师会面的父母的 NF1 知识得分也更高(p<0.001)。与 NF1 相关的癌症相关项目最不可能被正确回答。本研究结果表明,受影响父母的 NF1 总体知识水平较低,存在知识空白,表明有针对性的 NF1 教育可能会受益。