Mucopolysaccharidoses | National Institute of Neurological …
2024年7月19日 · Mucopolysaccharidoses (MPS) are a group of rare inherited metabolic diseases. There are many different types of MPS which present a variety of physical and neurological …
Mucopolysaccharidoses (MPS) - Johns Hopkins Medicine
What is mucopolysaccharidoses? Mucopolysaccharidoses is a group of genetic disorders — Hurler; Hunter; Sanfilippo A, B, C and D; Morquio A, B and C; and Maroteaux–Lamy — …
Mucopolysaccharidosis - Wikipedia
Mucopolysaccharidoses are a group of metabolic disorders caused by the absence or malfunctioning of lysosomal enzymes needed to break down molecules called …
Hurler Syndrome - Cleveland Clinic
Hurler syndrome is the most severe form of mucopolysaccharidosis type I, a hereditary lysosomal storage condition. Cells can't break down sugar molecules, which affects how they function. …
Mucopolysaccharidoses - Symptoms, Causes, Treatment | NORD
The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders. Lysosomes function as the primary digestive units within cells. Enzymes within lysosomes …
Mucopolysaccharidosis I (MPS I) - Hurler Syndrome and Scheie ... - WebMD
2023年9月4日 · MPS I stands for mucopolysaccharidosis type I. It starts in childhood. You can't "catch" it -- it comes from your genes. People with MPS I can't make a specific protein called …
Mucopolysaccharidosis type I - Wikipedia
Mucopolysaccharidosis type I is a spectrum of diseases in the mucopolysaccharidosis family. It results in the buildup of glycosaminoglycans (or GAGs, or mucopolysaccharides) due to a …
Mucopolysaccharidosis Type 1 (MPS 1) - Children's Hospital of Philadelphia
Mucopolysaccharidosis type 1 (MPS 1) is a rare lysosomal storage disease, which is an inherited metabolic disease characterized by an abnormal build-up of various toxic materials in the …
MPS I - National MPS Society
MPS I (Hurler-Scheie) is a continuum of severity based upon the symptoms, ranging from severe to attenuated. There is a great deal of variability of symptoms among individuals with MPS I, …
Mucopolysaccharidosis type I: MedlinePlus Medical Encyclopedia
2023年4月24日 · Mucopolysaccharidosis type I (MPS I) is a rare disease in which the body is missing or does not have enough of an enzyme needed to break down long chains of sugar …