For clinicians

Information for Healthcare Professionals on CDG

Diagnosis of any type of Congenital disorders of glycosylation (CDG) is still very rare and some heathcare professionals are still unfamiliar with either diagnosis or current research.

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Clinical Guidelines for CDG

Below are three sets of clinical guidelines available for free download:

• International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up

• Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation

• International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): Diagnosis, follow-up, and management

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You can also visit the CDG Care website to get updates for healthcare professionals.

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We work in partnership with the Portuguese Association CDG and Rare Metabolic Diseases (APCDG-DMR), a global voice to fight the impact of Rare Metabolic Diseases on affected individuals and their families. Every two years they host the World Conferences on CDG for healthcare professionals and families.

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Learn more from APCDG.

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Want to know about the latest research? Visit the APCDG website.