Erschienen in:
17.10.2023 | Letter to the Editor
Parkinsonism with prominent neuropsychiatric symptoms without pyramidal involvement in a patient with FBXO7 variants
verfasst von:
Surbhi Mahajan, Shivangi Mehta, Jagdeep Singh, Sahil Mehta, Vivek Lal
Erschienen in:
Neurological Sciences
|
Ausgabe 3/2024
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Excerpt
FBXO7 (F-box only protein 7) is a member of the F-box-containing protein family and plays a role in ubiquitin-mediated proteasomal degradation. FBXO7 mutations are a rare cause of autosomal recessive Parkinson’s disease and have been reported in the literature to produce a pallidopyramidal phenotype [
1]. We report a patient with compound heterozygous mutations in the FBX07 gene who presented with early-onset parkinsonism and prominent neuropsychiatric symptoms but without pyramidal involvement clinically. …