Two Pediatric Bone Disorders in the Era of Disease Specific Therapies – When to Refer Patients and How to Treat XLH and HPP

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Overview / Abstract:

Target Audience

This activity is designed to meet the educational needs of pediatricians in endocrinology, primary care, rheumatology, orthopedics, neurology, radiology, nephrology, neonatology, and other speciaties. Healthcare providers including geneticists and genetic counselors are included.

Program Overview

X-linked hypophosphatemia (XLH) and hypophosphotasia (HPP) are genetic metabolic bone diseases with recent treatment advances. This program will discuss when to refer and how to treat children with XLH or HPP in the era of disease specific therapies.

Learning Objectives

Upon completion of this activity, participants should be better able to:

Review pathophysiology, presentation, and diagnosis of hypophosphatasia (HPP) and X-linked hypophosphatemia (XLH) in children.
Evaluate the mechanisms, efficacy, and safety of agents approved for the treatment of HPP and XLH
Develop personalized strategies for the long-term management of children with HPP and XLH.

Expiration

Jun 21, 2023

Discipline(s)

Nursing CNE, Pharmacy CPE, Physician CME, Physician Assistant CME

Format

Online

Credits / Hours

1.0 AMA PRA Category 1 Credit(s)™

Accreditation

ACCME

Presenters / Authors / Faculty

Faculty

FACULTY_NAME
Jill H. Simmons, MD
Dr. Jill Simmons is a Professor of Pediatrics in the Ian M. Burr Division of Pediatric Endocrinology and Diabetes at Vanderbilt University Medical Center. She is the founder and director of the Vanderbilt Program for Pediatric Metabolic Bone Disease.

Dr. Simmons is an investigator of clinical trials on novel therapies for metabolic bone diseases in children. She authored numerous publications on the diagnosis and treatment of diseases including hypophosphatasia and X-linked hypophosphatemia. She serves as a regular reviewer for Diabetes Care, Journal of Clinical Endocrinology and Metabolism, Journal of Clinical Investigation, Pediatric Blood and Cancer, and Pediatric Diabetes.

FACULTY_NAME
Eric T. Rush, MD
Dr. Eric Rush is a Clinical Geneticist at Children’s Mercy Hospital and an Associate Professor of Pediatrics at the University of Missouri-Kansas City. He is the co-director of the Children’s Mercy Skeletal Dysplasia clinic.

Dr. Rush’s clinical and research interests include hypophosphatasia and X-linked hypophosphatemia, among others. Topics of his publications ranged from molecular characterization, skeletal pathology, to best practice of using novel therapies in rare genetic diseases. Dr. Rush is board certified in Pediatrics, Internal Medicine and Clinical Genetics. He is on the Scientific Advisory Board for the Rare Bone Diseases Alliance.

Sponsors / Supporters / Grant Providers

Alexion and Ultragenix.

Keywords / Search Terms

Relias LLC Relias LLC., FreeCME., Bone Disorders Free CE CME

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