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Genetic testing of the ATP7B gene can establish a definitive diagnosis and is valuable for family screening ( WD should be considered in the differential diagnosis of patients presenting with arthritis, particularly when accompanied by abnormal liver function tests

The diagnosis of AMS involves a complex scoring of clinical symptoms, incorporating subjectivity and intricate pathophysiology, which consequently leads to heterogeneity in genetic association studies

Examples of such substances include ammonium citrate, pepsin, phenobarbitone, sodium bromide, sodium iodide, potassium citrate, zinc chloride etc

Appointments are recommended to ensure dedicated time with a licensed provider