The first meeting of the group took place in Manchester in 1992, with five patients and their families in attendance.
Over the years numbers have increased dramatically, mainly due to the accessibility of the internet and the various links we have forged with healthcare practitioners within the NHS. We are now in contact with over 350 patients and their families in the UK. Many more people from countries across the world also look to us for information about the many aspects of the condition.
Official Charity Status was granted in March 2003.
We are supported by a team of Medical Advisors comprising healthcare professionals from across a range of disciplines. We are grateful for their continuing support.
Originally produced by Professor P. A. Farndon, Clinical Geneticist, Jim Costello (deceased) and Margaret Costello. We are reliant on a team of medical advisors for the clinical content of the website. We are grateful for their continuing support.
Gorlin Syndrome Group is Registered Charity in the UK - No 1096361