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Huntingtonova choroba

Heslo	Huntingtonova choroba
Heslo anglicky	Huntington Disease
Odkazy	Huntingtonova chorea Huntingtonova choroba juvenilná Huntingtonova choroba, akineticko-rigidný variant chorea progresívna hereditárna chronická (Huntington) chorea progresívna dedičná chronická (Huntington) Huntingtonova progresívna hereditárna chronická chorea Huntingtonova progresívna dedičná chronická chorea Huntingtonova choroba, juvenilná Huntingtonova choroba, s nástupom v ranom veku Huntingtonova choroba, s nástupom v neskoršom veku Huntingtonova choroba, s neskorším nástupom
Angl. X odkazy	Huntington Chorea Juvenile Huntington Disease
Vysvetľujúca pozn. v angl.	A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)
Odkazy	(45) - ČLÁNKY
	(5) - CiBaMed
	(16) - KNIHY

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