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Parkinson Disease

  • Matt BowerEmail author
  • Paul Tuite
Chapter

Abstract

Parkinson disease (PD), the second most-common neurodegenerative disease, is characterized by tremor, bradykinesia, and muscle rigidity. These characteristics, parkinsonism, may also be found in related diseases known as the Parkinson’s plus disorders and may be a component of numerous Mendelian conditions. The variety of inheritance patterns in familial parkinsonism includes autosomal dominant, autosomal recessive, autosomal dominant with reduced penetrance, and increased susceptibility due to risk genes. Additionally since PD is a common disorder, family history can be complicated by the co-occurrence of both the genetic and sporadic forms of the disease in the same pedigree.

Keywords

Genetic Counselor Deep Brain Stimulation Parkinson Disease Multiple System Atrophy Progressive Supranuclear Palsy 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Supplementary material

Parkinson’s disease Part 1 (MOV 360670 kb)

Parkinson’s disease Part 2 (MOV 190980 kb)

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Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  1. 1.Department of Genetics and MetabolismUniversity of Minnesota Medical Center, FairviewMinneapolisUSA
  2. 2.Department of NeurologyUniversity of Minnesota Medical Center, FairviewMinneapolisUSA

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