Lysosomal Storage Disorders: Recognizing and Addressing a Group of Rare Conditions

Learn about the various manifestations of lysosomal storage disorders (LSDs). Gaucher disease is one of the most common LSDs; others include Fabry disease, Niemann-Pick disease, and Pompe disease. These rare, inherited diseases can present with a range of symptoms and disease severity, making them difficult to diagnose. In fact, patients may go years without a correct diagnosis and appropriate treatment, leading to a cycle of multiple misdirected referrals, unnecessary procedures, delayed diagnosis and treatment, and disease progression. In this activity, 2 LSD experts discuss disease identification, diagnostic testing, and therapeutic strategies currently available and under investigation. Downloadable slides are also available to review and share with your colleagues. 

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Activities

  • Lysosomal Storage Disorders
    Lysosomal Storage Disorders: Recognizing and Addressing a Group of Rare Conditions
    Video
    Congratulations: You achieved a completion on 04/09/2022

    Released: December 12, 2022

    Expires: December 11, 2023

  • Lysosomal Storage Disorders
    Lysosomal Storage Disorders: Recognizing and Addressing a Group of Rare Conditions
    Slideset Download
    Congratulations: You achieved a completion on 04/09/2022

    Released: December 13, 2022

    Expires: December 12, 2023

Faculty

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Sarah Viall, MSN, PPCNP-BC

Assistant Professor
Department of Molecular and Medical Genetics/Department of Pediatrics
Oregon Health and Science University School of Medicine
Portland, Oregon

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Neal Weinreb, MD, FACP

Voluntary Associate Professor
Division of Human Genetics
University of Miami Miller School of Medicine
Miami, Florida

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Provided by Partners for Advancing Clinical Education 

Supporters

This activity is supported by an educational grant from 

Sanofi