1. Wilson Disease
Amanda Waltman
Christopher De Miranda
Michelle Pinto- Martinez
David Draper
Period 2
Group 5

2. What is Wilson Disease ?
 Wilsons disease is a rare genetic disease that requires the
patient to inherit two abnormal copies of the gene ATP7B. In
other words both parents must be carriers (have one abnormal
copy of this gene).
 The chances of getting this disease is about 1 in 40,000 people
world wide. The chances of being a carrier is about 1 in 90.
 It affects men, women and all races equally.
 Wilson disease Is a genetic disorder that prevents the body from
expelling excess copper.
 Copper builds up in the liver, brain, kidneys, and eyes. Over time
the copper causes irreversible organ damage.
 If left untreated this can be fatal.

3. Signs & Symptoms
Liver
 swelling of the liver or spleen
 jaundice, or yellowing of the skin and whites of the eyes
 fluid buildup in the legs or abdomen
 a tendency to bruise easily
 Fatigue
Neurologic
 problems with speech, swallowing, or physical coordination
 tremors or uncontrolled movements
 muscle stiffness
 behavioral changes
Other
 Anemia
 low platelet or white blood cell count
 slower blood clotting, measured by a blood test
 high levels of amino acids, protein, uric acid, and carbohydrates in urine
 premature osteoporosis and arthritis

4. Kayser-Fleischer Rings
 Kayser-Fleischer rings are brown/gold rings (generally a little
lighter than rust) that form around the edge of the iris and
cornea.
 They appear in both eyes
 Caused by copper deposits in stroma.

5. When do symptoms appear? Where does it affect?
 Symptoms generally
 It affects the liver, brain,
appear between ages 6 to
kidneys and eyes.
40, but can start as early
as 2 and as late as 72.  In the eyes it affects the
iris, cornea, and stroma.
 When you see symptoms
may depend on your diet

6. What causes Wilson Disease?
 Wilson disease is caused by the inability to filter copper from
the body.
 This is brought on by two pairs of mutated ATP7B gene.
 Copper builds up over time inside the body, causing copper
damage.

7. Diagnosis
 Wilson disease is diagnosed by a number of laboratory and
physical test.
 They look for Kayser-ischer rings. A special light called a slit
lamp is used to look for Kayser-Fleischer rings in the eyes.
Kayser-Fleischer rings are present in almost all people with
Wilson disease who show signs of neurologic damage but are
present in only 50 percent of those with signs of liver damage
alone
 Laboratory test measure the amount of copper in the blood
stream.

8. Treatment
 The first thing they do is remove the excess copper in the
body.
 The drugs d-penicillamine (Cuprimine) and trientine
hydrochloride (Syprine) release copper from organs into the
bloodstream.
 People with Wilson disease should reduce their dietary
copper intake. They should not eat shellfish or liver, as these
foods may contain high levels of copper
 Pregnant women should take a lower dose of d-penicillamine
or trientine hydrochloride during pregnancy to reduce the risk
of birth defects

9. Resources
 Schilsky, M.D, M. (2009, May ). Wilson Disease. Retrieved from
http://digestive.niddk.nih.gov/ddiseases/pubs/wilson/
 Mayo Clinic Staff. (2011, August 2). Wilson's disease. Retrieved
from http://www.mayoclinic.com/health/AboutThisSite/AM00057
 K Gilroy, R., & Katz, J. (2011, December 9). Wilson disease .
Retrieved from http://emedicine.medscape.com/article/183456-
overview
 Lorincz, M., & Huq, M. (2011, March 29). Wilson disease.
Retrieved from http://www.medlink.com/medlinkcontent.asp