Title |
Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome)
|
---|---|
Published in |
Cochrane database of systematic reviews, January 2014
|
DOI | 10.1002/14651858.cd008185.pub3 |
Pubmed ID | |
Authors |
da Silva, Edina MK, Strufaldi, Maria Wany Louzada, Andriolo, Régis B, Silva, Laercio A |
Abstract |
Mucopolysaccharidosis II, also known as Hunter syndrome, is a rare, X-linked disease caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase, which catalyses a step in the catabolism of glycosaminoglycans. The glycosaminoglycans accumulate within tissues affecting multiple organs and physiologic systems. The clinical manifestations include neurologic involvement, severe airways obstruction, skeletal deformities and cardiomyopathy. The disease has a variable age of onset and variable rate of progression. In those with severe disease, death usually occurs in the second decade of life, whereas those patients with less severe disease may survive into adulthood. Enzyme replacement therapy with intravenous infusions of idursulfase has emerged as a new treatment for mucopolysaccharidosis type II. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 2 | 100% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Scientists | 1 | 50% |
Members of the public | 1 | 50% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Colombia | 1 | 2% |
Unknown | 53 | 98% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Bachelor | 12 | 22% |
Researcher | 7 | 13% |
Student > Doctoral Student | 6 | 11% |
Student > Master | 6 | 11% |
Student > Postgraduate | 5 | 9% |
Other | 11 | 20% |
Unknown | 7 | 13% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 29 | 54% |
Biochemistry, Genetics and Molecular Biology | 3 | 6% |
Nursing and Health Professions | 3 | 6% |
Agricultural and Biological Sciences | 3 | 6% |
Psychology | 3 | 6% |
Other | 5 | 9% |
Unknown | 8 | 15% |