Our licenses grant only permissions under copyright and certain other rights that a licensor has authority to grant.Use of the licensed material may still be restricted for other reasons, including because others have copyright or other rights in the material.HD is an autosomal dominant inherited disease caused by an elongated CAG repeat (36 repeats or more) on the short arm of chromosome 4p16.3 in the Huntingtine gene.
The classic sign is chorea that gradually spreads to all muscles.
All psychomotor processes become severely retarded. Patients experience psychiatric symptoms and cognitive decline.
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