Wilson disease is a rare inherited disorder that causes copper to accumulate in the liver, brain, and other vital organs. Due to its low prevalence and highly variable clinical presentation, with symptoms that overlap more common disorders, patients are frequently misdiagnosed and encounter delays in diagnosis and treatment. Patients with Wilson disease require lifelong treatment. Standard-of-care therapies are associated with numerous adverse events, highlighting the need for safer therapies. Novel therapies currently under investigation have the potential to address several unmet needs in the management of Wilson disease. The second program in this series of 3 webinars will review the clinical manifestations of Wilson disease and strategies for diagnostic workup.
The goal of this activity is for learners to be better able to recognize the clinical manifestations of Wilson disease to enhance timely identification in clinical practice.
Upon completion of this activity, participants will: Have increased knowledge regarding the [LIST] [ITEM]Clinical manifestations of Wilson disease to raise index of suspicion [ITEM]Diagnostic workup for suspected Wilson disease[/LIST]
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[bold]For Physicians[/bold] Medscape, LLC designates this live activity for a maximum of 0.50 [italic][bold]AMA PRA Category 1 Credit(s)™[/bold][/italic]. Physicians should claim only the credit commensurate with the extent of their participation in the activity.