Literature DB >> 2968784

Presymptomatic neuropsychological impairment in Huntington's disease.

G W Jason1, E M Pajurkova, O Suchowersky, J Hewitt, C Hilbert, J Reed, M R Hayden.   

Abstract

Ten asymptomatic individuals at risk for Huntington's disease (HD) were determined by the use of linked DNA probes to have a high (HD+ group) or low (HD- group) probability of having inherited the mutant gene. Neuropsychological examination, performed without knowledge of DNA results, revealed impairments in five of seven subjects in the HD+ group. Abnormalities were related to visuospatial abilities or to functions associated with the frontal lobes. All three subjects in the HD- group showed no neuropsychological impairment. Statistical analyses confirmed differences between the HD+ and HD- groups. Affected parents of subjects were at least 12 years older at symptom onset. These results demonstrate that clear neuropsychological impairment may be present in HD even when overt signs and symptoms are not expected for a number of years.

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Year:  1988        PMID: 2968784     DOI: 10.1001/archneur.1988.00520310079021

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  18 in total

1.  Intelligence indices in people with a high/low risk for developing Huntington's disease.

Authors:  G M de Boo; A Tibben; J B Lanser; A Jennekens-Schinkel; J Hermans; M Vegter-van der Vlis; R A Roos
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  Visual processing disorders in patients with Huntington's disease and asymptomatic carriers.

Authors:  E Gómez-Tortosa; A del Barrio; T Barroso; P J García Ruiz
Journal:  J Neurol       Date:  1996-03       Impact factor: 4.849

3.  Neural bases of dysphoria in early Huntington's disease.

Authors:  Sergio Paradiso; Beth M Turner; Jane S Paulsen; Ricardo Jorge; Laura L Boles Ponto; Robert G Robinson
Journal:  Psychiatry Res       Date:  2008-01-15       Impact factor: 3.222

4.  Comparative assessment of the disorders of higher brain functions in various types of cerebral atrophy.

Authors:  I V Damulin; N N Yakhno; O A Goncharov
Journal:  Neurosci Behav Physiol       Date:  1991 Sep-Oct

Review 5.  Impairment of visuospatial function in idiopathic spasmodic torticollis.

Authors:  P Hinse; B Leplow; T Humbert; U Lamparter; A Junge; T Emskötter
Journal:  J Neurol       Date:  1996-01       Impact factor: 4.849

6.  Neuropsychological stability over two years in asymptomatic carriers of the Huntington's disease mutation.

Authors:  J R Campodonico; A M Codori; J Brandt
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-12       Impact factor: 10.154

7.  Decreased N-acetyl-aspartate/choline ratio and increased lactate in the frontal lobe of patients with Huntington's disease: a proton magnetic resonance spectroscopy study.

Authors:  L Harms; H Meierkord; G Timm; L Pfeiffer; A C Ludolph
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-01       Impact factor: 10.154

8.  Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers.

Authors:  V Hahn-Barma; B Deweer; A Dürr; C Dodé; J Feingold; B Pillon; Y Agid; A Brice; B Dubois
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-02       Impact factor: 10.154

9.  Neuropsychological characteristics of Huntington's disease carriers: a double blind study.

Authors:  N K Rosenberg; S A Sørensen; A L Christensen
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

10.  Cognitive changes in patients with Huntington's disease (HD) and asymptomatic carriers of the HD mutation--a longitudinal follow-up study.

Authors:  Jurgen Lemiere; Marleen Decruyenaere; Gery Evers-Kiebooms; Erik Vandenbussche; Rene Dom
Journal:  J Neurol       Date:  2004-08       Impact factor: 4.849

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