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Petrosillo, G., Moro, N., Ruggiero, F

124,125 Another example of genetic primary astrocytopathy is the Duchenne muscular dystrophy (DMD) caused by mutations in the gene encoding dystrophin, which in the CNS is present almost exclusively in astrocytes

PD is well know to affect movement, producing motor symptoms, and also to cause non-motor symptoms, which include autonomic dysfunction, neuropsychiatric problems (mood, cognition, behavior or thought alterations, personality changes, etc.), and sensory and sleep difficulties