An Overview of the Genetics of Parkinson's Disease

Author:

Aimrane Abdelmohcine1,Sabir Es-Said2ORCID,Laadraoui Jawad2ORCID,El-Mansoury Bilal2,Smimih Kamal3,Khanouchi Manal2,El Amine Souad2,Lafhal Karima2,Oublal Karima2,El Baz Soraia4,Mountassir Meriem2,Saad Fatima Ez-Zahraa2,Draoui Ahmed5ORCID,Abdelmonaim El Hidan Moulay2,Ferssiwi Abdessalam2,Bitar Abdelali2,Fdil Naima2

Affiliation:

1. Faculty of Sciences Semlalia, University Cadi Ayyad, Marrakech, Morocco

2. Independent Researcher, Morocco

3. Faculty of Sciences and Techniques, Sultan Moulay Slimane University, Mococco

4. Laboratory BioMagE, Labeled Unit-CNRST N°4, FSSM,UCA, Morocco

5. Faculty of Sciences Semlalia, Cadi Ayyad University, Morocco

Abstract

While the etiology of Parkinson's disease (PD) in most cases remains unknown, 10-15% of PD patients show a prognosis of monogenic forms of the disease with classical Mendelian type of inheritance. Indeed, the identified causative mutations contribute to dopaminergic neurons degeneration. In spite of the rarity of the genetic forms of PD, new molecular pathways are likely to be identified which are relevant in the sporadic form as well. In this chapter, the authors represent an update on the most relevant advances in the genetics of PD.

Publisher

IGI Global

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