Society guideline links: Gaucher disease

Introduction — This topic includes links to society and government-sponsored guidelines from selected countries and regions around the world. We will update these links periodically; newer versions of some guidelines may be available on each society's website. Some societies may require users to log in to access their guidelines.

The recommendations in the following guidelines may vary from those that appear in UpToDate topic reviews. Readers who are looking for UpToDate topic reviews should use the UpToDate search box to find the relevant content.

International

●Recommendations for the assessment and monitoring of skeletal manifestations in children with Gaucher disease (2008)

●International Collaborative Gaucher Group (ICCG): Gaucher disease type 1 – Revised recommendations on evaluations and monitoring for adult patients (2004)

United States

●American College of Medical Genetics (ACMG): Standards and guidelines on lysosomal storage diseases – Diagnostic confirmation and management of presymptomatic individuals (2011)

●Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease – Consensus recommendations (2004)

Europe

●European Working Group on Gaucher Disease (EWGGD): Management goals for type 1 Gaucher disease – An expert consensus document (2018)

●EWGGD: Management of neuronopathic Gaucher disease – Revised recommendations (2009)

India

●Society for Indian Academy of Medical Genetics and Indian Academy of Pediatrics (IAP): Diagnosis and management of Gaucher disease in India – Consensus guidelines (2018)