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Systemic Symptoms in Huntington's Disease: A Comprehensive Review
Raja Mehanna1, Joseph Jankovic2
1Department of Neurology, University of Texas Health Science Center at Houston, McGovern Medical School, Houston, TX, USA.
Huntington's disease (HD) affects the whole body, not just the brain. This review highlights systemic non-motor symptoms in HD patients, revealing a broader impact beyond typical motor, cognitive, and psychiatric issues.
Area of Science:
- Neurology
- Genetics
- Systemic Illness
Background:
- Huntington's disease (HD) is increasingly recognized as a systemic illness impacting the entire body.
- Beyond the classic triad of motor, cognitive, and psychiatric symptoms, HD involves widespread physiological effects.
Purpose of the Study:
- To review and highlight the systemic, non-motor symptoms associated with Huntington's disease.
- To draw attention to the full spectrum of HD's impact on patient health.
Main Methods:
- Systematic literature search of MEDLINE (1966-2023) using keywords related to Huntington's disease and systemic/autonomic symptoms.
- Critical review of 123 articles focusing on cardiovascular, respiratory, gastrointestinal, urinary, sexual, and cutaneous manifestations.
Main Results:
- Identified numerous systemic and autonomic co-morbidities in Huntington's disease patients.
- Observed that these co-morbidities do not always correlate with HD symptom severity or CAG repeat length.
Conclusions:
- Huntington's disease presents with diverse systemic and autonomic co-morbidities.
- Further research is essential to elucidate the pathophysiology and develop effective treatments for these systemic dysfunctions in HD.
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