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Cedars Sinai 15th Annual Lysosomal Storage Disease Symposium 2025

Cedars Sinai 15th Annual Lysosomal Storage Disease Symposium 2025

Regular price $29.00 USD
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Multi Speciality

No

Primary Speciality

Other-Specialized

Target Audience

physicians, geneticists, neurologists, pediatricians

Content Type

Mixed (Video + PDF)

Size

Mixed (Video + PDF)

Year

Provider/Organization

Other

  • Target Audience: physicians, geneticists, neurologists, pediatricians
  • Sample video: contact me for sample video
  • Information:

Target Audience

Specialties – ALL

Professions – Dietitian (Registered Dietitian), Genetic Counselor, Licensed Social Worker, Nurse, Nurse (Advanced Practice NP CRNA CNM CNS), Occupational Therapist, Pharmacist, Physical Therapist, Physician, Physician Assistant, Researcher (non-physician), Researcher (physician)

Overview

This continuing medical education conference provides a comprehensive update on lysosomal storage disorders (LSDs) for multidisciplinary healthcare teams. LSDs are genetic conditions caused by deficiencies in lysosomal components, primarily enzymes, which lead to lysosomal dysfunction and have widespread effects on peripheral organs and the central nervous system. Participants will explore the latest advances in the identification and diagnosis of LSDs, as well as current understanding of their pathophysiology. The course will also cover updates on management strategies and treatment options, emphasizing the translation of scientific breakthroughs into clinical practice. Expert faculty will present various clinical cases for discussion, along with research updates and case reports that highlight recent developments in the field. This conference aims to enhance the ability of healthcare professionals to provide optimal care for patients with these rare but debilitating disorders, equipping attendees with up-to-date knowledge to improve early diagnosis, implement appropriate management plans, and incorporate emerging therapies into their clinical practice.

Objectives

Apply updated knowledge of lysosomal storage disorders to improve diagnostic accuracy, develop prognoses, contribute to research, and enhance patient care

Identify the association between Gaucher disease and cancer

Describe the benefits, risks and limitations of newborn screening for lysosomal storage disorders in California

Analyze and integrate knowledge of Lysosomal Storage Disorders (LSDs) to collaborate effectively within interprofessional teams, facilitating improved patient care outcomes.

The Cedars-Sinai 15th Annual Lysosomal Storage Disease Symposium 2025 is best for physicians, geneticists, neurologists, pediatricians, and multidisciplinary healthcare providers who manage patients with lysosomal storage disorders (LSDs). It provides updates on diagnosis, treatment, and research advances, making it especially valuable for clinicians working in metabolic medicine, neurology, pediatrics, and rare disease care.

Who Should Attend

Physicians & specialists in neurology, pediatrics, internal medicine, and genetics.

Metabolic disease experts managing LSDs such as Gaucher, Fabry, Pompe, and MPS disorders.

Advanced practice providers (NPs, PAs) working in rare disease or neurology clinics.

Researchers & academic faculty studying lysosomal biology and therapeutic innovations.

Multidisciplinary teams (nurses, pharmacists, therapists) involved in patient care.

What You’ll Learn

Latest advances in LSDs: updates on pathophysiology, genetics, and clinical manifestations.

Therapeutic innovations: enzyme replacement therapy, substrate reduction, gene therapy.

Multisystem involvement: neurological, cardiac, skeletal, and visceral complications.

Case‑based learning: practical approaches to diagnosis and long‑term management.

Future directions: clinical trials, biomarkers, and personalized medicine strategies.

  • Topics:

Recording.mp4

Welcome and Introduction.pdf

Breakthroughs in Treatment for LSDs.pdf

Cancer in Gaucher Disease.pdf

Clinical Case 1.pdf

Clinical Case 2.pdf

Gaucher Disease – Clinical Updates.pdf

Gaucher Disease – Research Updates.pdf

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