Number of the records: 1  

Huntingtonova choroba

  1. Record numberd006816
    Date06.06.2025
    TypeM - MESH
    Topical termHuntingtonova choroba
    Other termEnglish (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
    UDCC10.228.140.079.545C10.228.140.380.278C10.228.662.262.249.750C10.574.500.497C16.320.400.430F03.615.250.400F03.615.400.390
    NoteA 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)
    subject heading

    subject heading

Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.