Ontology highlight
ABSTRACT:
SUBMITTER: Malinova V
PROVIDER: S-EPMC3509916 | biostudies-literature | 2012
REPOSITORIES: biostudies-literature
Malinová Věra V Węgrzyn Grzegorz G Narajczyk Magdalena M
JIMD reports 20111211
Mucopolysaccharidoses (MPS) are severe, inherited metabolic disorders caused by storage of glycosaminoglycans (GAGs). Sanfilippo disease (mucopolysaccharidosis type III, MPS III) is described as severe neurological type of MPS, characterized by rapid deterioration of brain functions. No therapy for Sanfilippo disease is approved to date, however, a specific substrate reduction therapy (SRT), called gene expression-targeted isoflavone therapy (GET IT), has been used as an experimental therapy. In ...[more]