BACKGROUND : 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 patients increasingly survive to adulthood and undergo multiple surgeries throughout their lives. As surgeries in these patients are considered to be high risk, this can result in a range of critical clinical situations in adult patients. RESULTS : We discuss strategies to prepare for and manage critical clinical situations in adult patients with MPS, including supporting the multidisciplinary team, preoperative and airway assessments, surgical preparations, and postoperative care. We also present eight critical clinica...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosom...
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosom...
Supplementary Information. Preoperative assessment.BACKGROUND : Mucopolysaccharidoses (MPS) are rare...
AbstractThe mucopolysaccharidoses are a group of inherited metabolic diseases caused by deficiencies...
Mucopolysaccharidoses (MPS) are rare disorders associated with enzyme deficiencies, resulting in gly...
textabstractMucopolysaccharidosis type II (MPS II) is a rare, life-limiting, X-linked recessive dise...
Abstract Mucopolysaccharidoses (MPS) are genetic, progressive, lysosomal storage disorders affecting...
Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glyco...
The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders with clinical m...
Introduction: Mucopolysaccharidosis (MPS) VI or Maroteaux-Lamy syndrome (253200) is an autosomal rec...
International audienceMucopolysaccharidoses are a group of rare lysosomal storage diseases including...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
Purpose. Mucopolysaccharidoses (MPS) are group of inherited lysosomal storage diseases caused by mut...
Selva, Erica M.Mason, Robert W.Tomatsu, ShunjiMucopolysaccharidoses (MPS) are lysosomal storage diso...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosom...
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosom...
Supplementary Information. Preoperative assessment.BACKGROUND : Mucopolysaccharidoses (MPS) are rare...
AbstractThe mucopolysaccharidoses are a group of inherited metabolic diseases caused by deficiencies...
Mucopolysaccharidoses (MPS) are rare disorders associated with enzyme deficiencies, resulting in gly...
textabstractMucopolysaccharidosis type II (MPS II) is a rare, life-limiting, X-linked recessive dise...
Abstract Mucopolysaccharidoses (MPS) are genetic, progressive, lysosomal storage disorders affecting...
Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glyco...
The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders with clinical m...
Introduction: Mucopolysaccharidosis (MPS) VI or Maroteaux-Lamy syndrome (253200) is an autosomal rec...
International audienceMucopolysaccharidoses are a group of rare lysosomal storage diseases including...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
Purpose. Mucopolysaccharidoses (MPS) are group of inherited lysosomal storage diseases caused by mut...
Selva, Erica M.Mason, Robert W.Tomatsu, ShunjiMucopolysaccharidoses (MPS) are lysosomal storage diso...
Mucopolysaccharidoses (MPS) represent a group of rare lysosomal storage disorders, with a heterogene...
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosom...
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosom...