Wilson disease
A very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.
Also known as: Westphal-Strumpell syndrome, Wilson disease, Wilson's disease, hepatolenticular degeneration, WD.
Category: General
Drugs labeled for Wilson disease
2 medication ingredients list an association with wilson disease in current FDA labeling.
Symptoms associated with Wilson disease
The following symptoms have been associated with Wilson disease in medical literature. Not everyone experiences the same symptoms.
Abdominal distention
Distention of the abdomen....
Dysphagia
Difficulty in swallowing....
Edema
An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body....
Hand tremor
An unintentional, oscillating to-and-fro muscle movement affecting the hand....
Hypoesthesia
Decreased ability to perceive touch....
Insomnia
Persistent difficulty in starting or maintaining sleep, or waking up earlier than desired, despite having adeq...
Jaundice
Yellow pigmentation of the skin due to bilirubin, which in turn is the result of increased bilirubin concentra...
Limb muscle weakness
Reduced strength and weakness of the muscles of the arms and legs....
Pedal edema
An abnormal accumulation of excess fluid in the lower extremity resulting in swelling of the feet and extendin...
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Tremor
An unintentional, oscillating to-and-fro muscle movement about a joint axis....
Vomiting
Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic...
Tests used to investigate Wilson disease
Healthcare providers may order these tests when evaluating Wilson disease. Test selection is a clinical decision made by a qualified professional.
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Comprehensive Metabolic Panel (CMP)
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...
Urinalysis
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....
Conditions with overlapping symptoms
These conditions share symptoms with Wilson disease, which is why a clinical evaluation is important.
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Frequently Asked Questions
What is Wilson disease?
Wilson disease is a health condition described in medical literature. A very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.
What are the symptoms of Wilson disease?
Wilson disease is associated with 12 symptoms in the medical literature we index, including Abdominal distention, Dysphagia, Edema, Hand tremor, Hypoesthesia, Insomnia. Symptoms vary widely between individuals.
How is Wilson disease diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Wilson disease include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.
Is SymptomDatabase.com diagnosing me?
No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have Wilson disease, please discuss your symptoms with a qualified healthcare provider.