eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | huntington disease |
| Symptom | C0426980|motor symptoms |
| Sentences | 6 |
| PubMedID- 22761268 | In addition to motor symptoms, patients with huntington disease or other choreic disorders often experience increasing depression, bradykinesia, cognitive impairment, aggressive behaviors, and other complications as the disease progresses. |
| PubMedID- 22387017 | Age at the onset of motor symptoms in huntington disease (hd) is determined largely by the length of a cag repeat expansion in htt but is also influenced by other genetic factors. |
| PubMedID- 26407011 | Aim: pridopidine, a new oral drug for treatment of patients with motor symptoms associated with huntington's disease (hd) is currently under development. |
| PubMedID- 20645403 | motor symptoms in huntington's disease (hd) are commonly assessed by the unified huntington's disease rating scale-total motor score (uhdrs-tms). |
| PubMedID- 20144006 | Background: as an effect of the cognitive, emotional and motor symptoms associated with huntington's disease, communicative interaction is often dramatically changed. |
| PubMedID- 25562602 | This model has been used to explain the motor symptoms of parkinson's disease, huntington's disease, and other neurological disorders associated with basal ganglia dysfunction. |
Page: 1