Critical clinical situations in adult patients with Mucopolysaccharidoses (MPS)

Mucopolysaccharidoses (MPS) are rare, inherited disorders associated with enzyme deficiencies that result in glycosaminoglycan (GAG) accumulation in multiple organ systems. Management of MPS is evolving as pat...

Source: Orphanet Journal of Rare Diseases - May 14, 2020 Category: Internal Medicine Authors: Karolina M. Stepien, Anait K. Gevorkyan, Christian J. Hendriksz, Tinatin V. Lobzhanidze, Jordi P érez-López, Govind Tol, Mireia del Toro Riera, Nato D. Vashakmadze and Christina Lampe Tags: Research Source Type: research