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X-linked hypophosphatemia (XLH) is the most common genetic form of rickets, characterized by stunted growth with disproportionate short stature, bowing of the lower limbs associated with reduced motor skills, osteoarticular pain, hypotonia, and dental and periodontal anomalies. Recently developed global treatment guidelines based on GRADEd methodology and endorsed by several global organizations, including the ASBMR, have ushered in opportunities to better diagnose and treat patients with this life-long bone disease. Join us as we discuss actual patient cases using the new guidelines demonstrating improvement in patient diagnosis and outcomes.
Schedule |
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| * Times are PST | |
| 12:45 PM | Luncheon |
| 12:55 PM | Welcome, Disclosures, Supporter Acknowledgement |
| 01:00 PM | Pediatric and Adult Patient Cases Clinical Presentation, Diagnosis, and Complications |
| 01:30 PM | Disease Progression Monitoring and Management |
| 01:45 PM | Closing Comments, Audience Q&A |
| 02:00 PM | Adjourn |
Aliya Khan, MD, FRCPC, FACP, FASBMR
Professor of Clinical Medicine
Divisions of Endocrinology and Geriatrics
Director, Calcium Disorders Clinic
McMaster University
Hamilton, ON, Canada
David R. Weber, MD, MSCE
Medical Director, Center for Bone Health
Children’s Hospital of Philadelphia (CHOP)
Associate Professor of Pediatrics
University of Pennsylvania Perelman School of Medicine
Philadelphia, PA
Thomas J. Weber, MD
Medical Director, Duke Clinical Bone Laboratory
Professor of Medicine
Division of Endocrinology, Metabolism, and Nutrition
Duke University Medical Center
Durham, NC
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EXCEL Continuing Education designates this live activity for a maximum of 1.0 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
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