The need for early identification makes
Hunter disease a candidate for new-born screening (NBS).
Tedesco et al., "Enzymatic replacement therapy for
Hunter disease: up to 9 years experience with 17 patients," Molecular Genetics and Metabolism Reports, vol.
At just seventeen years old, Daniel Muers touched hundreds of hearts as he fought the incurable
Hunter Disease, so rare that just 40 babies are born with the condition in the UK every decade.
In this report, we describe a new assay for mucopolysaccharidosis II (MPS-II) (
Hunter disease) that uses MS/MS and DBSs.
David is one of the first sufferers of the metabolic disorder
Hunter Disease or MPS II to go on a ground breaking trial which is offering sufferers hope of a cure.
The youngster is battling
Hunter Disease, so rare that just 40 babies are born with it in the UK every decade.
Daniel, nine, from Heaton, has
Hunter Disease, which causes his joints to stiffen up.
Brave Daniel Muers, nine, from High Heaton, who has
Hunter Disease, received a tricycle.