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• W2147078172 abstract "<b>Background:</b> The combination of early-onset, progressive parkinsonism with pyramidal tract signs has been known as pallido-pyramidal or parkinsonian-pyramidal syndrome since the first description by Davison in 1954. Very recently, a locus was mapped in a single family with an overlapping phenotype, and an <i>FBXO7</i> gene mutation was nominated as the likely disease cause. <b>Methods:</b> We performed clinical and genetic studies in two families with early-onset, progressive parkinsonism and pyramidal tract signs. <b>Results:</b> An <i>FBXO7</i> homozygous truncating mutation (Arg498Stop) was found in an Italian family, while compound heterozygous mutations (a splice-site IVS7 + 1G/T mutation and a missense Thr22Met mutation) were present in a Dutch family. We also found evidence of expression of novel normal splice-variants of <i>FBXO7</i>. The phenotype associated with <i>FBXO7</i> mutations consisted of early-onset, progressive parkinsonism and pyramidal tract signs, thereby matching clinically the pallido-pyramidal syndrome of Davison. The parkinsonism exhibits varying degrees of levodopa responsiveness in different patients. <b>Conclusions:</b> We conclusively show that recessive <i>FBXO7</i> mutations cause progressive neurodegeneration with extrapyramidal and pyramidal system involvement, delineating a novel genetically defined entity that we propose to designate as <i>PARK15</i>. Understanding how <i>FBXO7</i> mutations cause disease will shed further light on the molecular mechanisms of neurodegeneration, with potential implications also for more common forms of parkinsonism, such as Parkinson disease and multiple system atrophy." @default.
• W2147078172 created "2016-06-24" @default.
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• W2147078172 date "2008-11-26" @default.
• W2147078172 modified "2023-10-06" @default.
• W2147078172 title "FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome" @default.
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• W2147078172 doi "https://doi.org/10.1212/01.wnl.0000338144.10967.2b" @default.
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