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1
Intro
2
Historical Perspectives
3
Current Understanding
4
Epidemiology
5
"Prodromal" Stage
6
Early Motor Signs of HD
7
EARLY COGNITIVE CHANGES
8
Other Early Symptoms of HD
9
Progression of Motor Symptoms
10
General Treatment Principles
11
CARE IS MULTIDISCIPLINARY
12
Combination Therapies
13
MEDICATIONS FOR CHOREA
14
MEDICATIONS FOR MOOD
15
MEDICATIONS FOR COGNITION
16
DONEPEZIL: NO IMPROVEMENT
17
End of Life Issues
18
Caregiving in HD
Description:
Explore the diagnosis, stages, and treatment of Huntington's disease in this comprehensive lecture by Dr. Veronica Santini, Clinical Instructor at Stanford University Medical Center. Delve into the historical perspectives, current understanding, and epidemiology of this rare genetic disorder that causes programmed degeneration of brain cells. Learn about the "prodromal" stage, early motor signs, cognitive changes, and other early symptoms. Examine the progression of motor symptoms, general treatment principles, and multidisciplinary care approaches. Discover combination therapies and medications for chorea, mood, and cognition. Gain insights into end-of-life issues and caregiving in Huntington's disease. This talk, presented by the Stanford Huntington's Disease and Ataxia Clinic, a Center of Excellence recognized by the Huntington's Disease Society of America, reflects the high treatment standards offered at Stanford.

Huntington's Disease - Stages and Therapies

Stanford University
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