Case report: Early-onset Parkinson’s disease with lower limb spasticity in a new DJ-1/PARK7 patient

Masako Fujita, H. Nishijima, Atsuko Katagai, Chieko Suzuki, Nobutaka Hattori, M. Tomiyama
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Abstract

Rare autosomal recessive variants in DJ-1, a causative gene for early-onset Parkinson’s disease, have been associated with a variety of clinical syndromes in a limited number of patients. Here, we report a case of a novel DJ-1 variant in a 39-year-old man with a 4-year history of parkinsonism, cognitive dysfunction, and lower limb spasticity. He was diagnosed with Parkinson’s disease. Genetic testing of the patient revealed compound heterozygous variants in the DJ-1 gene (exon 6 deletion + c.242dup), of which exon 6 deletion was a novel variant. We conclude that variants in DJ-1 should be considered possible causes of early-onset parkinsonism with spasticity and cognitive impairment, as in this case.
病例报告:一名 DJ-1/PARK7 新患者伴有下肢痉挛的早发性帕金森病
DJ-1是早发性帕金森病的致病基因,其罕见的常染色体隐性变异与少数患者的多种临床综合征有关。在此,我们报告了一例新型 DJ-1 变异,患者是一名 39 岁的男性,有 4 年的帕金森病史、认知功能障碍和下肢痉挛。他被诊断为帕金森病。对该患者的基因检测发现了 DJ-1 基因的复合杂合变异(外显子 6 缺失 + c.242dup),其中外显子 6 缺失是一种新型变异。我们的结论是,DJ-1基因变异应被视为本病例这种伴有痉挛和认知障碍的早发性帕金森病的可能病因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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