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Young-Onset Parkinson’s Disease with Impulse Control Disorder Due to Novel Variants of F-Box Only Protein 7

机译:由于F-Box的新型变异仅限蛋白质7幼眼帕金森病了脉冲控制障碍

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摘要

F-box only protein 7 (FBXO7) is a rare monogenic cause of hereditary Parkinson’s disease (PD) with an autosomal recessive mode of inheritance and a broad spectrum of clinical manifestations. Here, we report a de novo PD patient with onset at the age of 28 with novel compound heterozygous variants in the FBXO7 gene (c.1162C>T, p.Gln388X; c.80G>A, p.Arg27His). The clinical features of the patient were problematic impulse control disorder behaviors and pyromania, and pyramidal signs were negative. We describe the novel pathogenic variants of the FBXO7 gene with detailed clinical pictures to report the expanding genotypes and phenotypes of FBXO7-associated parkinsonism.
机译:F型盒仅蛋白质7(FBXO7)是遗传性帕金森病(Pd)的罕见单一的异常原因,具有常染色体隐性遗传模式和广谱的临床表现。在这里,我们在28岁时报告了迄今为止发病的DE Novo PD患者,其中FBXO7基因中的新化合物杂合变体(C.1162C> T,P.Gln388x; C.80G> A,P.Arg27His)。患者的临床特征是有问题的脉冲控制障碍行为和吡喃症,金字塔迹象是阴性的。我们描述了FBXO7基因的新致病变体,具有详细的临床图片,以报告FBXO7相关帕金森主义的扩张基因型和表型。

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