Subject(s)
Blepharoptosis/genetics , Dwarfism/genetics , Hypertrichosis/genetics , Intellectual Disability/genetics , Mutation/genetics , Phospholipases/genetics , Retinitis Pigmentosa/genetics , Adolescent , Blepharoptosis/diagnostic imaging , Cerebellum/diagnostic imaging , Developmental Disabilities/diagnostic imaging , Developmental Disabilities/genetics , Dwarfism/diagnostic imaging , Female , Humans , Hypertrichosis/diagnostic imaging , Intellectual Disability/diagnostic imaging , Magnetic Resonance Imaging , Retinitis Pigmentosa/diagnostic imaging , Tomography Scanners, X-Ray ComputedABSTRACT
The functional characterization of identified disease genes in monogenic forms of Parkinson's disease (PD) allows first insights into molecular pathways leading to neurodegeneration and dysfunction of the nigrostriatal system. There is increasing evidence that disturbance of the ubiquitin proteasome pathway is one important feature of this process underscoring the relevance of protein misfolding and accumulation in the neurodegenerative process of PD. Other genes are involved in mitochondrial homeostasis and still others link newly identified signalling pathways to the established paradigm of oxidative stress in PD. Additional factors are posttranslational modifications of key proteins such as phosphorylation. Also, molecular data support the role of altered iron metabolism in PD. Here we describe known genes and novel genetic susceptibility factors and define their role in neurodegeneration.
