patients.gi.org/topics/wilson-disease Wilson disease is a very treatable condition. With proper therapy, disease progress can be halted and oftentimes symptoms can be improved. Left untreated, Wilson disease may be fatal.
en.wikipedia.org/wiki/Wilson%27s_disease Wilson's disease or hepatolenticular degeneration is an autosomal recessive genetic disorder in which copper accumulates in tissues; this manifests as neurological or psychiatric symptoms and liver disease.
www.wilsonsdisease.org/wilson-disease/wilsondisease... Wilson disease is a very treatable condition. With proper therapy, disease progress can be halted and oftentimes symptoms can be improved. Treatment is aimed at removing excess accumulated copper and preventing its reaccumulation.
www.patientslikeme.com/conditions/288-wilson-disease Wilson Disease: Find the most comprehensive real-world symptom and treatment data on Wilson Disease at PatientsLikeMe. 22 patients with Wilson Disease experience Anxious mood, Pain, Insomnia, Fatigue, and Depressed mood.
www.patient.co.uk/health/wilsons-disease What is Wilson's disease? Wilson's disease is a condition where too much copper builds up in the body. It is a rare inherited disorder that affects about 1 in 30,000 people.
emedicine.medscape.com/article/183456 Wilson disease is a rare autosomal recessive inherited disorder of copper metabolism. The condition is characterized by excessive deposition of copper in the liver, brain, and other tissues.
www.liverfoundation.org/abouttheliver/info/wilson Almost all patients with Wilson’s Disease also have a decreased level of serum ceruloplasmin, a copper binding protein, in their blood. An increase of copper in the urine is present in most but not all patients, and corneal Kayser-Fleischer rings are present in 50% of people with the disease.
www.ncbi.nlm.nih.gov/pubmed/17433323 Late-onset Wilson's disease. Ferenci P, Członkowska A, Merle U, Ferenc S, Gromadzka G ... The diagnostic features and the frequency of late-onset WD gene mutations were not different than in patients with an earlier onset of disease. Factors other than ATP7B mutations may modify the phenotypic ...
www.ncbi.nlm.nih.gov/pmc/articles/PMC3383125 Wilson's disease is an autosomal recessive disorder affecting copper transport; it results in the accumulation of copper in the liver, brain, and other organs.
www.medindia.net/patients/patientinfo/wilsons-disease... Wilson's Disease requires lifelong treatment. If the disorder is detected early and treated correctly, a person with Wilson's disease can enjoy completely normal health, but without proper treatment, Wilson's is generally fatal.
www.uptodate.com/contents/wilson-disease-treatment-and... Wilson disease (hepatolenticular degeneration) is an autosomal recessive defect of cellularcopperexport. Reduced biliary excretion leads to accumulation of copper, initially in the liver and then in other tissues, particularly the brain. Tissue coppe
www.rightdiagnosis.com/w/wilsons_disease/symptoms.htm Symptoms of Wilson's Disease including 84 medical symptoms and signs of Wilson's Disease, alternative diagnoses, misdiagnosis, and correct diagnosis for Wilson's Disease signs or Wilson's Disease symptoms.
emedicine.medscape.com/article/183456-workup The presence of Kayser-Fleischer rings and ceruloplasmin levels of less than 20 mg/dL in a patient with neurologic signs or symptoms suggest a diagnosis of Wilson disease.
www.uptodate.com/contents/wilson-disease-clinical... Wilson disease (hepatolenticular degeneration) is due to a genetic abnormality inherited in an autosomal recessive manner that leads to impairment of cellularcoppertransport. It is found worldwide, with a prevalence of approximately 1 case in 30,000
www.rightdiagnosis.com/w/wilsons_disease/intro.htm Wilson's Disease: Introduction. Wilson's disease is a disorder in which there is a high level of copper that accumulates in the liver and other organs.
www.liverdoctor.com/liver-problems/wilson-disease Wilson Disease is a very rare inherited disorder causing an inability of the body to metabolize the mineral copper. It results in very high and toxic levels of copper building up in the liver and parts of the brain, leading to liver scarring (cirrhosis) and neurolo
books.google.com/.../Wilson_s_Disease_for_the_Patient_and...... Wilson's Disease for the Patient and Family: A Patients Guide to Wilson's disease and Frequently asked Questions about Copper, is an essential reference book for patients with Wilson's disease and their families. In easily understood language, Dr. George J. Brewer, a world authority on Wilson's ...
www.barnesandnoble.com/w/wilsons-disease-for-the-patient... Wilson's Disease for the Patient and Family: A Patient's Guide to Wilson's Disease and Frequently Asked Questions about Copper by; M. D. George J. Brewer,
labtestsonline.org/understanding/conditions/wilsons What is Wilson disease? Wilson disease is an inherited genetic disorder associated with abnormal copper metabolism that results in excess storage of copper, primarily in the liver and brain.
wilsondisease.net/wilsondisease-patients.php The WDA provides a caring community that will offer each Wilson disease family information, guidance and emotional support. We are dedicated to education, advancing treatments, and finding a cure for Wilson disease.
www.arizonadigestivehealth.com/low-copper...wilsons-disease Background: Wilson’s disease, also called hepatolenticular degeneration, is a hereditary disorder that affects the body’s ability to regulate its copper absorption and storage.
www.nlm.nih.gov/medlineplus/wilsondisease.html Wilson disease is a rare inherited disorder that prevents your body from getting rid of extra copper. You need a small amount of copper from food to stay healthy.
www.sciencedirect.com/science/article/pii/S2210740114000576 Since Wilson disease (WD) may not be present with evident clinical symptoms of liver injury and neurological presentation is rare in children, establishing a di
www.gwumc.edu/edu/obgyn/genetics/casestudies/casestudy33.htm... CSF fluid will have a copper concentration 3-4 times higher than in Wilson’s disease patients with no neurological involvement. These levels usually fall with appropriate treatment. ...
www.sciencedirect.com/science/article/pii/S0006291X06009533 Wilson disease (WD) is an autosomal recessive disorder of copper metabolism, which is caused by mutation in copper-transporting ATPase (ATP7B). In the present s
www.easl.eu/assets/application/files/e793d591ec4de1c... EASL Clinical Practice Guidelines: Wilson’s disease European Association for the Study of the Liver⇑ Summary This Clinical Practice Guideline (CPG) has been developed to
www.cincinnatichildrens.org/health/w/wilsons Wilson's disease is a rare inherited disease that is caused by having too much copper in the body. Copper is a substance found in many foods and in drinking water.
www.encyclopedia.com/topic/Wilsons_disease.aspx Wilson Disease Definition. Wilson disease, or WD, is a rare inherited disorder that causes excess copper to accumulate in the body. It is also known as hepatolenticular degeneration.
www.amazon.com/Wilsons-Disease-Patient-Family-Frequently... Amazon.com: Wilson's Disease for the Patient and Family:A Patient's Guide to Wilson's Disease and Frequently Asked Questions about Copper eBook: George J.: Kindle Store
www.meja.aub.edu.lb/downloads/19_4/21-WILSONS.pdf patient with Wilson’s disease. Middle East J Anesthesiol; 11:391-7, 1992. 3. CUELLO AZCARATE JJ, GARCIA HERNANDEZ E, GONZALEZ RODRIGUEZ JL: Epidural anesthesia and analgesia in a patient with cerebral manifestations of Wilson’s disease.
www.nytimes.com/health/guides/disease/wilsons-disease/... Wilson's disease is an inherited disorder in which there is too much copper in the body's tissues. The excess copper damages the liver and nervous system.