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Wilson Disease
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Published on Nov 06, 2015
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PRESENTATION OUTLINE
1.
WILSON DISEASE
Jeremy Stirmel
2.
SYMPTOMS
Jaundice-skin turns yellow or other white parts of your eyes
Low levels of white blood cells
Low levels of red blood cells
High levels of protein, amino acids and uris acids in the urine
Swelling in the abdomen
3.
TREATMENT
Removing the excess copper from the body
Reducing intake of foods that are rich in copper
Treating any liver or central nervous system damage
Reduce the amount of copper in a normal diet
For Wilson Disease you will need life long treatment.
4.
Inheritance
To inherit Wilson Disease you will need to inherit mutated copies of a gene-one form each parent.
5.
IMPACT ON FAMILY
This disorder may cause fatal impacts of the liver
Difficulty moving arms and legs
Weakness
Tremors in the hands and feet
The symptoms may not be fatal but may leave many disabled body parts
6.
SOURCES
http://www.genome.gov/27532725
http://digestive.niddk.nih.gov/ddiseases/pubs/wilson/#treatment
http://www.ninds.nih.gov/disorders/wilsons/wilsons.htm
7.
Research on Wilson Disease
The NIH show the design for better therapies for this disorder.
Jeremy S
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