Genetic condition awaiting consideration - Walker Warburg Syndrome Muscular dystrophydystroglycanopathy type A, 1
Walker Warburg Syndrome is an autosomal recessive congenital muscular dystrophy with associated brain and eye abnormalities.
The condition is normally lethal within the first few months of life with most individuals dying by 3yrs.
Have your say on conditions awaiting consideration
If you have any feedback on the genetic conditions awaiting consideration by the HFEA, send us an email and we will discuss your comments at the next Licence Committee.
Email your feedback to: pgd@hfea.gov.uk
You can also sign up to our PGD update email alert service which will keep you up to date, on a monthly basis, with information on the latest conditions added to the authorised list and conditions that are awaiting approval about which you can provide comments.
Page last updated: 16 July 2012