Wilson’s disease, or copper disease, is a rare disorder marked by elevated copper levels in different body areas, including the liver, brain, and eyes. Copper is consumed through diet and is essential for many body functions, including the immune system, nerve function, and the production of red blood cells. However, excessive copper buildup can result in organ damage and other potentially fatal issues.
Liver:
Eye:
Neuropsychiatric symptoms :
Some additional signs of Wilson’s disease include kidney problems, anemia, osteoporosis, or the appearance of blue nails.
The diagnosis of Wilson’s disease is quite challenging, as parents with a single mutated gene are carriers to their children but often remain asymptomatic. Furthermore, even though the condition is congenital, the child may not exhibit symptoms until they are five years old or much older. However, Wilson’s disease can be ruled out with the help of standard diagnostic procedures like liver enzyme tests, blood and urine tests to measure copper levels, and imaging tests like MRIs, CT scans, and liver biopsies. Early identification and accurate diagnosis based on the person’s symptoms can stop copper toxicity through optimal treatment plans & appropriate care.
Senior Consultant Neurologist and Programme Director-PDMDRC
Senior Consultant Neurologist & Clinical Director
Sr. Consultant Neurosurgeon-PDMDRC, Clinical Director-PDMDRC.
Sr. Consultant Neurologist, Clinical Director- PDMDRC ( Parkinson’s Disease and Movement Disorders Research Centre)
Consultant Neurologist
Consultant Neurologist, Consultant PDMDRC
Consultant Neurologist
Consultant Neurologist
Consultant Neurologist
Senior Consultant Neurologist
Consultant Neurologist
Consultant Neuro Physician
Consultant Neurologist & Epileptologist
Consultant Neurologist & Head-Cerebrovascular Unit
Consultant Neuro Physician
Associate Consultant Neurosurgeon
Sr. Consultant Neuro Physician, HOD, Department of Neurology
Sr. Consultant Neuro Physician
Consultant Neurologist
Consultant Neurophysician
Consultant Neuro Physician
Talk to Our Health Care Experts!
Through early identification and appropriate therapy, the symptoms associated with Wilson’s disease can be effectively managed, reducing the chances of additional complications and allowing individuals to lead lives similar to others.
Since Wilson’s disease is associated with gene mutations, the cure for it is quite challenging; however, if it is identified in the early stages and the liver is not severely damaged, it can be managed with medications, and quality of life can be significantly improved.
The liver is the most affected organ in Wilson’s disease, & so fatty liver is a common manifestation of this condition. However, it is often misdiagnosed as non-alcoholic fatty liver disease. It is crucial to conduct further tests, such as genetic assessments, serum ceruloplasmin levels (the copper transport protein), a 24-hour urine test, and a liver biopsy to identify Wilson’s disease at an early stage.
Appointment
Second Opinion
Live Chat
Call
More
