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This book covers recent developments and possible pitfalls in the diagnosis of genetic movement disorders and related conditions. It is divided into three sections: technical and scientific aspects; clinical aspects with guidance towards work-up; and ethical and legal aspects of genetic testing in a clinical and research setting. The first section includes chapters on genetic analysis and counselling with critical discussion of potential problems when interpreting the results. Clinical chapters summarize genetic forms of movement disorders including parkinsonism, tics and dystonia with algorithms for hands-on daily practice. Related conditions such as RLS, ataxias and dementias are also covered. Finally, chapters on ethical and legal aspects of genetic testing are included. Movement Disorder Genetics is aimed at clinicians and scientists working in the field of movement disorders and related conditions.
Table of Content
Genetics of Mendelian Forms of Parkinson’s Disease
Lesage, Suzanne, Seiten 3-18
Genetics of Parkinson’s Disease
Hernandez, Dena G. (et al.), Seiten 19-34
Genetics of Atypical Parkinsonism
Stamelou, Maria (et al.), Seiten 35-64
Genetics of Dementia with Lewy Bodies
Brás, José M. Tomás, Seiten 65-74
Genetics of Frontotemporal Dementia
Heetveld, Sasja (et al.), Seiten 75-105
Genetics of Primary Tremor Disorders
Kuhlenbäumer, Gregor, Seiten 107-123
Genetics of Dystonia
Schneider, Susanne A. (et al.), Seiten 125-146
Genetic Choreas
Walker, Ruth H. (et al.), Seiten 147-167
Genetics of Tourette Syndrome
Lennington, Jessica B. (et al.), Seiten 169-189
Genetics of Paroxysmal Dyskinesia
Brockmann, Knut (et al.), Seiten 191-211
Genetics of Dominant Ataxias
Manto, Mario (et al.), Seiten 213-233
Genetics of Recessive Ataxias
Klebe, Stephan (et al.), Seiten 235-261
Genetics of NBIA Disorders
Wiethoff, Sarah (et al.), Seiten 263-291
Genetics of Metal Disorders (Excluding NBIA)
Dusek, Petr (et al.), Seiten 293-330
Genetics of Restless Legs Syndrome (RLS)
Schulte, Eva C. (et al.), Seiten 331-351
Genetics of Hereditary Spastic Paraplegias (HSP)
Schüle, Rebecca (et al.), Seiten 353-383
Genetics of ALS
McLaughlin, Russell Lewis (et al.), Seiten 385-409
Genetics of Mitochondrial Disease with Focus on Movement Disorders
Finsterer, Josef (et al.), Seiten 411-430
Genetic Testing, Interpretation of Genetic Test Reports and Genetic Counseling for Clinicians
Bennett, Robin L., Seiten 433-450
Genetic Testing: An Industrial Perspective
Hadaschik, Dirk (et al.), Seiten 451-462
Direct-to-Consumer DNA Genetic and Genomic Testing
Trent, Ronald J., Seiten 463-478
Current Ethical Issues Related to the Implementation of Whole-Exome and Whole-Genome Sequencing
Borry, Pascal (et al.), Seiten 481-497
Implications for Health and Life Insurances and Other Legal Aspects of Genetic Testing
Ngueng Feze, Ida (et al.), Seiten 499-519
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