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Huntington's Disease
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Published on Nov 20, 2015
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PRESENTATION OUTLINE
1.
SYMPTOMS
Usually develop at the ages of 30 to 50
Uncontrollable movement of arms, legs, head, face, and upper body
Decline in reasoning and thinking skills
Decline in memory, concentration,, judgement and ability
OCD
2.
TREATMENT
There is no known cure
Dopamine blockers help reduce behaviors and movements
Amantadine and tetrabenazine control extra movements
There is also no known way to slow its progression
3.
DISCOVERY
Discovered by Jonah Christian in 1860
First thorough description of it was by George Huntingtin
He found that it was genetically passed down
4.
OTHER
Those who had it before it's naming
We're believed it be witches
And possessed by demons
5.
LIFE EXPECTANCY
There is no way to tell how long someone will live with huntingtons
Patients can live anywhere from 10 to 30 years depending on the severity of symptoms
6.
HOW IT WORKS
It is a neurodegenerative genetic, single gene disorder
Passed down from parent to child
Nerve cells degenerate
Affects muscle coordination
Mutation of gene in chromosome 4
7.
Untitled Slide
8.
WHAT IT AFFECTS
It affects your nerve cells
Muscle coordination
Brain cells become toxic to other cells
9.
WHO IT EFFECTS
It affects parents who have it
Children of those who may have it
If a parent has Huntingtons there is a 50% chance of the child having it
10.
DIAGNOSIS
A neurological exam
Neurologists, genetic counselors
Social workers, psychiatrists
and psychologists exam someone who
Are approved for the exam
Chris Dingrando
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