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- W2068674554 abstract "Mucopolysaccharidoses (MPS) constitute, owing to their biochemical, genetical and clinical characteristics, a large and heterogeneous subgroup among the lysosomal storage diseases (LSD). They are caused by deficiency of specific enzymes, which are responsible for glycosaminoglycan (GAG) breakdown during different steps of its degradation pathway. MPS are responsible for about 32% of inborn errors of metabolism (IEM) and 54% of LSD identified in our laboratory (Regional Laboratory of Inborn Errors of Metabolism (RLIEM), Medical Genetics Unit, Hospital de Clínicas in Porto Alegre), which is a reference center for LSD diagnosis in Brazil. Therefore, we decided to set up a specific laboratory routine for detection and differential diagnosis of MPS in patients with clinical features suggestive of this group of disorders" @default.
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- W2068674554 date "1998-03-01" @default.
- W2068674554 modified "2023-10-16" @default.
- W2068674554 title "A useful routine for biochemical detection and diagnosis of mucopolysaccharidoses" @default.
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- W2068674554 doi "https://doi.org/10.1590/s1415-47571998000100028" @default.
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