Advanced diagnostics for MucopolysaccharidosesARCHIMEDlife News , Diagnostics December 7, 2020
Mucopolysaccharidoses (MPSs) are a group of inherited lysosomal storage disorders affecting lysosomal metabolism. MPSs result in the accumulation of glycosaminoglycans in the body and can… Read more
High incidence of α-Mannosidosis in ‘MPS-like’ phenotypesPublications , Diagnostics September 2, 2020
α-Mannosidosis is an inherited lysosomal storage disorder caused by genetic mutations leading to limited or no expression of a gene responsible for metabolizing oligosaccharides. Besides… Read more
First LEA assay launchedARCHIMEDlife News March 14, 2018LEA2 MPS Panel Our first LEA2 (Lysosomal Enzyme Activity) assay has now been started and with it several mucopolysaccharidoses (MPS) can be diagnosed from one… Read more
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