Abstract
Neurodevelopmental disorders with early-onset parkinsonism have diverse genetic aetiologies and can mimic Parkinson's disease. We report the clinical evaluation and neuroimaging studies of a woman with intellectual disability and levodopa-responsive akinetic rigid parkinsonism. Whole-genome sequencing of family trio identified a de novo missense variant in PPP2R5D in the proband.
Original language | English |
---|---|
Article number | 106976 |
Journal | Parkinsonism and Related Disorders |
Volume | 124 |
DOIs | |
Publication status | Published - Jul 2024 |