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Huntington's Disease
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Published on Nov 24, 2015
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PRESENTATION OUTLINE
1.
HUNTINGTON DISEASE
PATIENT DIAGNOSIS BY BRUCE BALES AND ZACHARY BATES
2.
SYMPTOMS
Difficulty with normal tasks
Hard time swallowing
Frequent muscle spasms
Hard time completing thoughts
3.
PATIENT INFO
40 years of age
Experiencing multiple symptoms of huntingtons
Is more than likely to have huntingtons
4.
IMPORTANT INFORMATION
3/7 of patients have European ancestry
There is a 50% chance that a child will inherit the disease
There is a 1-3% chance of developing the disease sporadically
Autosomal dominant gene
Depression and suicide are common
5.
TREATMENT
Dopamine blockers
Tetrabenazine
Amantadine
6.
PROGNOSIS
Symptoms should be closely monitored
24-hour care may be necessary
15-20 year lifespan expected
7.
GENETICS
Autosomal dominant inheritance
Can be acquired spontaniously
8.
SOURCES
Patient.co.uk
Kumc.edu
Ghr.nlm.nih.gov
Nervous-system.emedtv.com
Nytimes.com
9.
SOURCES
Patient.co.uk
Kumc.edu
Ghr.nlm.nih.gov
Nervous-system.emedtv.com
Nytimes.com
Ailsa Beggs
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