Commentary on: A new genetic variant, presenting as young onset rapidly progressive dementia and parkinsonism

In September edition of Movement Disorders Rounds, Dr. Negin Eissazade et al. describe an interesting young patient who developed a rapidly progressive parkinsonism and dementia syndrome secondary to a novel homozygous missense mutation in the alpha-synuclein (SNCA) gene [1].

Source: Parkinsonism and Related Disorders - March 21, 2024 Category: Neurology Authors: M. Claudia Uribe Roca Source Type: research