Počet záznamov: 1
Huntingtonova choroba
Č. záznamu d006816 Dátum 06.06.2025 Typ M - MESH Tematický termín Huntingtonova choroba Iný termín Angličtina (Pseudonym) Huntington Chorea
Angličtina (Pseudonym) Juvenile Huntington Disease
Slovenčina (Pseudonym) Huntingtonova chorea
Slovenčina (Pseudonym) Huntingtonova choroba juvenilná
Slovenčina (Pseudonym) Huntingtonova choroba, akineticko-rigidný variant
Slovenčina (Pseudonym) chorea progresívna hereditárna chronická (Huntington)
Slovenčina (Pseudonym) chorea progresívna dedičná chronická (Huntington)
Slovenčina (Pseudonym) Huntingtonova progresívna hereditárna chronická chorea
Slovenčina (Pseudonym) Huntingtonova progresívna dedičná chronická chorea
Slovenčina (Pseudonym) Huntingtonova choroba, juvenilná
so (Pseudonym) Huntingtonova choroba, s nástupom v detstve
Slovenčina (Pseudonym) Huntingtonova choroba, s nástupom v ranom veku
Slovenčina (Pseudonym) Huntingtonova choroba, s nástupom v neskoršom veku
Slovenčina (Pseudonym) Huntingtonova choroba, s neskorším nástupom
MDT 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 Poznámka 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) 
predmetové heslo
Počet záznamov: 1