Hunter disease

Hunter disease

[Charles H. Hunter, Canadian physician, 1873–1955]
Mucopolysaccharidosis II.
References in periodicals archive ?
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.
Long-term follow-up following bone marrow transplantation for Hunter Disease.
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.
Other examples include Tay-Sachs disease, Hunter disease and Pompe disease.
Eight-year-old Daniel Muers, of Thropton Terrace, High Heaton, is battling Hunter Disease, which affects only around 40 babies a decade in the UK.
TKT's Niche Protein product platform is based on protein replacement for the treatment of rare genetic diseases such as Fabry disease, Hunter disease and Gaucher disease, a group of disorders characterized by the absence of certain metabolic enzymes.
Money raised by the Run has helped youngsters such as Daniel Muers, seven, whose fight against the incurable Hunter Disease touched the hearts of Newcastle United's stars.
Daniel, seven, is battling the incurable Hunter Disease, so rare that just 40 babies are born with the condition in the UK every decade.