Hunter disease

[Charles H. Hunter, Canadian physician, 1873–1955]

Mentioned in ?

mucopolysaccharidosis II

References in periodicals archive ?

The need for early identification makes Hunter disease a candidate for new-born screening (NBS).

Clinical, Biochemical and Molecular Characteristics of Fifteen Patients with Mucopolysaccharidosis Type II in Western Turkey

Tedesco et al., "Enzymatic replacement therapy for Hunter disease: up to 9 years experience with 17 patients," Molecular Genetics and Metabolism Reports, vol.

Hunter Syndrome Diagnosed by Otorhinolaryngologist

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.

From Magpies to princes, they all loved Dan's smile

In this report, we describe a new assay for mucopolysaccharidosis II (MPS-II) (Hunter disease) that uses MS/MS and DBSs.

Tandem mass spectrometry for the direct assay of enzymes in dried blood spots: application to newborn screening for mucopolysaccharidosis II (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.

WHY DAVID HAS HOPE FOR A BETTER FUTURE

The youngster is battling Hunter Disease, so rare that just 40 babies are born with it in the UK every decade.

Family geared up for big charity bash

Daniel, nine, from Heaton, has Hunter Disease, which causes his joints to stiffen up.

Sunbeams

Brave Daniel Muers, nine, from High Heaton, who has Hunter Disease, received a tricycle.