About Us

The Gorlin Syndrome Group is a support network offering guidance and information to patients, their families and carers whose lives are affected by Gorlin Syndrome (also known as Nevoid Basal Cell Carcinoma Syndrome).  

The group is organised by patients affected by Gorlin Syndrome and their families, with support from medical advisors.

Our aims and objectives are:

  • to offer guidance and information to individuals, their carers, family and friends with Gorlin syndrome
  • the advancement of the education of the medical profession into Gorlin syndrome and its implications for the family
  • to promote research into the causes, effects, treatment and management of Gorlin syndrome.

We are grateful for the continuing support of medical advisors.

Interim Statement - We are currently in the process of updating all clinical information on the website.  If you require more detailed information/evidence then you can contact us via contact us

Every reasonable effort has been made to ensure the information on the Gorlin Syndrome Group website is up to date and accurate. The information is not a substitute for medical care, if you have worries about your condition then speak to a General Practitioner or healthcare professional.

The Gorlin Syndrome Group cannot be held responsible for the information on the website, neither can the Gorlin Syndrome Group be responsible for the content or accuracy provided on external web links.


 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 
 
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