Number of the records: 1
Huntingtonova choroba
Record number d006816 Date 06.06.2025 Type M - MESH Topical term Huntingtonova choroba Other term English (Pseudonym) Huntington Chorea
English (Pseudonym) Juvenile Huntington Disease
Slovak (Pseudonym) Huntingtonova chorea
Slovak (Pseudonym) Huntingtonova choroba juvenilná
Slovak (Pseudonym) Huntingtonova choroba, akineticko-rigidný variant
Slovak (Pseudonym) chorea progresívna hereditárna chronická (Huntington)
Slovak (Pseudonym) chorea progresívna dedičná chronická (Huntington)
Slovak (Pseudonym) Huntingtonova progresívna hereditárna chronická chorea
Slovak (Pseudonym) Huntingtonova progresívna dedičná chronická chorea
Slovak (Pseudonym) Huntingtonova choroba, juvenilná
so (Pseudonym) Huntingtonova choroba, s nástupom v detstve
Slovak (Pseudonym) Huntingtonova choroba, s nástupom v ranom veku
Slovak (Pseudonym) Huntingtonova choroba, s nástupom v neskoršom veku
Slovak (Pseudonym) Huntingtonova choroba, s neskorším nástupom
UDC C10.228.140.079.545C10.228.140.380.278C10.228.662.262.249.750C10.574.500.497C16.320.400.430F03.615.250.400F03.615.400.390 Note 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) 
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Number of the records: 1