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Phenotypic variability in chorea-acanthocytosis associated with novel VPS13A mutations

Citation

Niemelä, Valter et al. (2021), Phenotypic variability in chorea-acanthocytosis associated with novel VPS13A mutations, Dryad, Dataset, https://doi.org/10.5061/dryad.7h44j0zr9

Abstract

Objective: To perform a comprehensive characterization of a cohort of patients with chorea-acanthocytosis (ChAc) in Sweden.

Methods: Clinical assessments, targeted genetic studies, neuroimaging with MRI,18F-fluorodeoxyglucose (FDG) PET and dopamine transporter with [123I] FP-CIT (DaTscan) SPECT. One patient underwent Magnetic Resonance Spectroscopy (MRS).

Results: Four patients living in Sweden but with different ethnical backgrounds were included. Their clinical features were variable. Biallelic VPS13A mutations were confirmed in all patients, including three novel mutations. All tested patients had either low or absent chorein levels. One patient had progressive caudate atrophy. Investigation using FDG PET revealed severe bilateral striatal hypometabolism and DaTscan-SPECT displayed presynaptic dopaminergic deficiency in three patients. MRS demonstrated reduced N-acetylaspartate/creatine (NAA/Cr) ratio as well as mild elevation of both choline/creatine (Cho/Cr) and combined glutamate and glutamine /creatine (Glx/Cr) in the striatum in one case. One patient died during sleep, another was treated with DBS which transiently attenuated feeding dystonia but not his gait disorder or chorea.

Conclusions: Larger longitudinal neuroimaging studies with different modalities, particularly MRS, are needed in order to determine their potential role as biomarker/s for ChAc.

Funding

Region Stockholm

Region Stockholm