CME HOURS
ACA‐20260000174
This educational webinar is designed to enhance healthcare practitioners’ knowledge and clinical competency in the diagnosis and assessment of rare metabolic bone disorders. The program provides a structured overview of differential diagnosis principles, followed by focused, case-based discussions on hypophosphatasia, osteogenesis imperfecta, and osteomalacia/XLH. Interactive
knowledge assessments, including MCQs and a mock OSCE-style clinical exam, are incorporated to reinforce learning outcomes, evaluate clinical reasoning, and
support the application of evidence-based practices in clinical settings
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( 1 DAY )
Systematically apply evidence-based diagnostic frameworks to the evaluation of patients with suspected rare metabolic bone disorders, enabling accurate differentiation between overlapping clinical presentations within the scope of current international guidelines.
Critically analyze and interpret complex clinical cases of hypophosphatasia, osteogenesis imperfecta, and osteomalacia/XLH by integrating clinical findings, biochemical markers, and imaging results to support precise diagnosis and appropriate management planning.
Differentiate between inherited and acquired metabolic bone disorders through structured case-based discussions, enhancing diagnostic accuracy and reducing the risk of misdiagnosis in routine clinical practice.
Demonstrate improved clinical reasoning and knowledge retention in the field of metabolic bone diseases by achieving measurable competency through interactive MCQ-based assessments aligned with the educational content delivered during the webinar.
Apply standardized clinical assessment approaches in a simulated OSCE format to evaluate patients with suspected bone disorders, demonstrating competency in history taking, physical examination, diagnostic prioritization, and clinical decision-making.
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Activity details