What is Wilson's disease?

Dec 01, 2025 Source: Cainiu Health
Dr. Gao Jun
Introduction
Hepatolenticular degeneration, commonly known as Wilson's disease, is a genetic disorder caused by impaired copper metabolism. Management should focus on controlling copper levels. It is essential to strictly limit high-copper foods in the diet, such as animal offal, nuts, shellfish, and other seafood, and instead choose low-copper ingredients. Patients must take prescribed copper-chelating medications as directed and must not discontinue or adjust the dosage without medical guidance.

Wilson's disease, commonly known as hepatolenticular degeneration, is a genetic disorder caused by impaired copper metabolism. The detailed analysis is as follows:

Wilson's disease is a condition resulting from inherited defects in copper metabolism. Genetic mutations impair the liver’s ability to properly excrete copper, leading to excessive accumulation of copper ions in organs such as the liver, brain, and kidneys, gradually damaging cellular functions. Early symptoms often involve liver abnormalities, such as fatigue and jaundice. As the disease progresses, neurological symptoms like limb tremors and slurred speech may appear. If left untreated, it can become life-threatening. However, early intervention can effectively control disease progression.

Management focuses on reducing copper levels. Diet should strictly limit high-copper foods, including animal organs, nuts, shellfish, and other seafood, while favoring low-copper alternatives. Patients must take prescribed copper-chelating medications as directed and must not discontinue or adjust dosages without medical guidance. Regular monitoring of copper levels and liver and kidney function is essential to allow timely adjustments to treatment. Maintaining a regular lifestyle, avoiding excessive fatigue that burdens the liver, and keeping emotional stability are also important. A healthy overall state helps maintain bodily functions and reduces the risk of complications.

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