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[Study on the clinical misdiagnosis of hepatolenticular degeneration]
1Hospital Affiliated to Institute of Neurology, Anhui College of TCM, Hefei 230061, China.
Insights
Hepatolenticular degeneration (HLD) is frequently misdiagnosed, delaying critical treatment. Early diagnosis significantly improves patient outcomes, highlighting the need for prompt identification and intervention for this rare genetic disorder.
Area of Science:
- Neurology
- Medical Diagnostics
- Genetics
Context:
- Hepatolenticular degeneration (HLD), also known as Wilson's disease, is a rare autosomal recessive genetic disorder.
- HLD affects copper metabolism, leading to copper accumulation in organs like the liver, brain, and eyes.
- Delayed diagnosis of HLD can result in severe, irreversible organ damage and neurological complications.
Purpose:
- To determine the incidence and patterns of misdiagnosis for hepatolenticular degeneration (HLD).
- To investigate the relationship between diagnostic delays and treatment outcomes in HLD patients.
- To identify strategies for improving the early detection and management of HLD.
Summary:
- Over 51% of 1,011 analyzed HLD cases were misdiagnosed, with nearly 20% lacking a specific diagnosis for over three months.
- Patients were misdiagnosed with over 100 conditions, including hepatitis, cirrhosis, and various neurological disorders.
- Early diagnosis (within three months) was associated with significantly better treatment outcomes compared to delayed or missed diagnoses (P < 0.01).
Impact:
- Highlights the critical need for increased awareness and diagnostic accuracy for HLD among clinicians.
- Emphasizes that prompt diagnosis and initiation of treatment are crucial for improving patient prognosis and preventing long-term complications.
- Suggests incorporating specific tests like Kayser-Fleischer (K-F) ring examination and copper metabolism tests for suspected HLD cases.
Objective:
To study the proportion and frequency of misdiagnosis of hepatolenticular degeneration (HLD), diseases easily confused with HLD, and the relation between misdiagnosis and curative effect so as to sum up experience and improve diagnosis.
Methods:
1 011 cases with the confirmed diagnosis of HLD who were hospitalized in the Hospital Affiliated to the Institute of Neurology, Anhui College of TCM from November 1993 to June 2000 were analyzed. Those patients who had attended two or more than two hospitals and had been misdiagnosed as other diseases or failed to get a clear diagnosis for 3 months and over before hospitalization were included in the group of clinical misdiagnosis or the group without a definite diagnosis. Relevant data were analyzed.
Results:
516 cases (51.04%) were misdiagnosed, 193 cases (19.09%) failed to be diagnosed as a specific disease, only 302 cases (29.87%) had been diagnosed as HLD within 3 months after the onset. The 516 cases had been misdiagnosed as more than 100 different diseases, including all types of hepatitis, cirrhosis, splenomegaly, hepatomegaly, arthritis, nephritis, encephalitis, encephalopathy, psychosis, anaemia, and so on. The curative effect was much better in the group with early diagnosis than in the groups with misdiagnosis and without a clear diagnosis (P < 0.01).
Conclusion:
HLD is often misdiagnosed as other diseases or fails to get a clear diagnosis. Early diagnosis and treatment without delay is critical to the prognosis. Patients with symptoms described in this article should be examined for the presence of corneal K-F ring and copper metabolism teat should be made when necessary.
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