The Development of National Clinical Guidelines and Integrated Care Pathways and Audit of Practices Against these Standards : A Collaborative Project Byall Scottish Clinical Genetics Services

In July 1996 a nationwide study was started in Scotland aiming to devise evidence based clinical guidelines for 5 genetic conditions- Tuberous Sclerosis (TS), Myotonic Dystrophy (MD), Marfan Syndrome, Huntington’s Disease (HD) and Neurofibromatosis 1 (NF1). To facilitate the use of the guidelines and audit of the clinical management of these conditions Care Pathways were devised from guidelines. This project was funded for three years by the Clinical Resource and Audit Group of the Scottish Office (CRAG).

Recommendation: Print and bring these guidelines and care plan when visiting your doctor. Ask them to review the Information.

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