Successful desensitization in a type VI mucopolysaccharidosis patient with probable IgE-mediated allergy to galsulfase [Naglazyme]
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Immunology and Allergy,Immunology
Reference8 articles.
1. Mucopolysaccharidosis VI;Valayannopoulos;Orphanet Journal of Rare Diseases,2010
2. Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study
3. Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase;Harmatz;Mol Genet Metab,2008
4. Skin testing for IgE-mediated drug allergy;Kränke;Immunol Allergy Clin North Am,2009
5. Immune response to enzyme replacement therapy: 4-sulfatase epitope reactivity of plasma antibodies from MPS VI cats;Turner;Mol Genet Metab,1999
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1. Allergic reactions to enzyme replacement therapy in children with lysosomal storage diseases and their management;Journal of Pediatric Endocrinology and Metabolism;2024-09-04
2. Abbreviation of Desensitization Protocol for Pediatric Patients with Lysosomal Storage Diseases Receiving Enzyme Replacement Therapy;International Archives of Allergy and Immunology;2024-07-17
3. Hypersensitivity reaction during enzyme replacement therapy in lysosomal storage disorders. A systematic review of desensitization strategies;Pediatric Allergy and Immunology;2023-06
4. Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux–Lamy syndrome ( MPS VI );American Journal of Medical Genetics Part A;2021-08-26
5. Management of hypersensitivity reactions to enzyme replacement therapy in children with lysosomal storage diseases;Annals of Allergy, Asthma & Immunology;2020-10
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