超声诊断弗雷泽综合征1例基因确认的必要性?

F. Golshahi, B. Moradi, Forough Jabbari, M. Ahmadi
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引用次数: 0

摘要

弗雷泽综合征是一种罕见的遗传性疾病,其特征是多种结构异常,其中最主要的是隐眼和并指。根据对报告病例的审查,已经确定了诊断标准。在此,我们报告一例妊娠18周诊断为弗雷泽综合征,在超声检查中表现为眼球隐型,并指畸形,肾脏发育不全和高回声肺部。终止妊娠,随后确认了该综合征的诊断特征。由于影像特征是独特的,临床医生熟悉该综合征的外观是有价值的,为家庭提供及时决定是否终止妊娠的机会,并使用产前诊断工具在随后的怀孕中拥有健康的孩子。
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A case of Fraser Syndrome Diagnosed by Ultrasound as a Single Modality; Necessity of Genetic Confirmation?
Fraser syndrome is a rare genetic disorder characterized by multiple structural abnormalities, above all of which are cryptophthalmos and syndactyly. According to reviews of reported cases, diagnostic criteria have been established. Here, we report a case of 18 weeks pregnancy diagnosed with Fraser syndrome presenting with cryptophthalmos, syndactyly, kidney agenesis, and hyper-echogenic lungs during an ultrasound examination. The pregnancy was terminated, and diagnostic features of the syndrome were confirmed afterward. Since the imaging characteristics are unique, it is of value that clinicians become familiar with the appearance of the syndrome to provide families with the opportunity to make timely decisions regarding pregnancy termination and use the prenatal diagnostic tools to have healthy children in subsequent pregnancies.
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