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Updated: Sep 1, 2026

Handwriting Analysis Indicates Spontaneous Dyskinesias in Neuroleptic Naïve Adolescents at High Risk for Psychosis
Published on: November 21, 2013
Bradykinesia in Huntington's disease
P J Garcia Ruiz1, E Gomez Tortosa, V Sanchez Bernados
1Department of Neurology, Fundacion Jimenez Diaz, Madrid, Spain.
Insights
Huntington's disease (HD) patients exhibit significant bradykinesia, performing worse than healthy controls and even Parkinson's disease patients on motor tasks. Motor impairment in HD correlates with disease severity.
Area of Science:
- Neurology
- Movement Disorders
Background:
- Huntington's disease (HD) is primarily known for hyperkinetic movements.
- However, bradykinesia (slowness of movement) is also a common feature in HD patients.
- Understanding the motor deficits in HD is crucial for diagnosis and management.
Purpose of the Study:
- To compare the motor performance of Huntington's disease patients with healthy controls and Parkinson's disease patients.
- To investigate the presence and severity of bradykinesia in HD.
- To determine the relationship between motor impairment and clinical stage in HD.
Main Methods:
- Evaluated motor performance in 18 genetically confirmed HD patients, 18 controls, and 20 Parkinson's disease (PD) patients.
- Utilized four standard PD timed motor tests: Pronation-Supination (PS), Finger Dexterity (FD), Movement Between Two Points (MTP), and Walking Test (WT).
- HD and PD groups were assessed under specific conditions (HD off neuroleptics, PD off medication).
Main Results:
- HD patients were significantly slower than controls across all motor tasks (p < 0.01).
- HD patients demonstrated slower performance than PD patients in finger dexterity (p < 0.05).
- All motor tests showed a significant positive correlation with the clinical stage of HD (r values ranging from 0.75 to 0.87).
Conclusions:
- Severe bradykinesia is a significant motor impairment in Huntington's disease.
- Motor deficits in HD are directly related to the clinical stage of the disease.
- HD patients exhibit profound motor slowing, comparable to or exceeding that seen in Parkinson's disease for certain tasks.
Abstract:
Huntington's disease (HD) is characterized by the presence of hyperkinesias, but bradykinesia is also present in most patients. We studied the motor performance of 18 patients with genetically proven HD (age, 38.5 +/- 10 y; clinical stage, 1.7 +/- 1.7; (CAG) triplet length, 49.2 +/- 6.8 triplets; all but three patients were free from neuroleptics) and compared with a control group (n = 18) and with a typical Parkinson's disease (PD) group (n = 20). Motor study included the four timed tests commonly used for PD: Pronation-supination (PS), finger dexterity (FD), movement between two points (MTP) and walking test (WT). Tests were done at 9 AM. The PD group was studied in "off" condition, with no medication given for 12 hours. The HD group was slower than the controls on all tasks (all tests significant, p < 0.01, Mann-Whitney U test) and even slower than PD group (for FD, p < 0.05). A significant correlation was found between each test and clinical stage (for PS, r = 0.84; for FD, r = 0.75; for MTP, r = 087, and for WT, r = 0.77, Pearson). Severe bradykinesia was present in HD, and motor impairment is related to clinical stage.
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