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StatPearls, LLC

  • Gaucher Disease
  • Osteoporosis
  • Pancytopenia

Gaucher Disease

Gaucher disease, the most prevalent lysosomal storage disorder, presents with an elevated incidence among Ashkenazi Jews. It is an autosomal recessive inborn error of metabolism characterized by the toxic accumulation of glucocerebroside lipids within multiple organs. Gaucher disease results from mutations in the GBA1 gene, leading to deficient glucocerebrosidase activity within lysosomes. Clinical manifestations, including hepatosplenomegaly, pancytopenia, osteoporosis, and avascular necrosis, vary in severity depending on the disease type. This activity comprehensively examines the assessment and management of Gaucher disease while emphasizing the pivotal role of the interprofessional team in collaborating and delivering well-coordinated care to improve patient outcomes.

Credit & MOC Details

Credit information is provided by the course provider. We recommend confirming credit eligibility with the provider or your licensing board before starting the activity.

Credit types

AAPA Category 1 Credit™Up to 1.5 creditsAMA PRA Category 1 Credit™Up to 1.5 creditsNursingUp to 1.5 creditsPharmacyUp to 1.5 credits

MOC types

ABS — Accredited CMEUp to 1.5 pointsABOS — Accredited CMEUp to 1.5 pointsABPATH — Lifelong LearningUp to 1.5 pointsABA — Lifelong LearningUp to 1.5 pointsABTS — Accredited CMEUp to 1.5 pointsABIM — Medical KnowledgeUp to 1.5 pointsABS — Self-AssessmentUp to 1.5 pointsABP — Lifelong Learning and Self-AssessmentUp to 1.5 pointsABTS — Self-AssessmentUp to 1.5 points

FDA REMS

No

Qualifies for MIPS

No

Target Specialties

Cross-Specialty

Relevant across 12 specialties.

Pricing

Fee varies

This provider typically $49–98

See fees on statpearls.com

Listed by the provider

  • Article / monograph / reference
  • Credit · Up to 1.5 credits
  • MOC · Up to 1.5 points
  • Fee varies · this provider typically $49–98
  • Released
    Sep 1, 2026
  • Last day to claim credit
    Sep 1, 2029 3 years left

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