Titlebook: Chorea; Causes and Managemen Federico E. Micheli,Peter A. LeWitt Book 2014 Springer-Verlag London 2014 chorea.choreiform disorder.cognitive

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Kapitel 8: Weiterführende Überlegungenians with them. While treatment remains symptomatic, advances have been made with genetic delineation. Hopefully with better understanding of their pathophysiology, we will also move towards mechanistic therapies.

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https://doi.org/10.1007/978-3-540-75516-6th other neurologic and extraneurologic symptoms. In these cases, family and clinical history, physical examination, and a specific set of ancillary studies such as genetic, neuroimaging, and biochemical studies will often enable a correct diagnosis.

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Huntington Disease and Huntington Disease-Like Syndromes: An Overview,ians with them. While treatment remains symptomatic, advances have been made with genetic delineation. Hopefully with better understanding of their pathophysiology, we will also move towards mechanistic therapies.

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Chorea in Childhood,th other neurologic and extraneurologic symptoms. In these cases, family and clinical history, physical examination, and a specific set of ancillary studies such as genetic, neuroimaging, and biochemical studies will often enable a correct diagnosis.

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ical management of the different choreic disorders.Update on.Chorea: Causes and Management. provides a comprehensive and timely update for the wide variety of neurological conditions, both inherited and acquired, which result in this common hyperkinetic movement disorder..This book describes in deta

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Chorea in Inherited Ataxias,ebellar ataxias (ARCAs), such as ataxia telangiectasia (more commonly), and Friedreich ataxia (more rarely). In the group of spinocerebellar ataxias (SCAs), chorea can be found more commonly in patients with SCA type 17, and in dentatorubral-pallidoluysian atrophy (DRPLA).