Hunter Syndrome (MPS II): Symptoms & Causes - Cleveland Clinic
Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a rare inherited lysosomal storage disorder. With MPS II, sugar molecules called glycosaminoglycans (GAGs) build up within the lysosomes of your child’s cells. This buildup causes damage that affects physical and mental development. What is Hunter syndrome?
Hunter syndrome - Wikipedia
Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a rare genetic disorder in which large sugar molecules called glycosaminoglycans (or GAGs or mucopolysaccharides) build up in body tissues. It is a form of lysosomal storage disease.
Hunter Syndrome: Symptoms, Causes, Diagnosis, and Treatment
2024年5月1日 · Hunter syndrome is an inherited genetic disorder that leads to the buildup of sugar molecules called GAGs. The buildup of these sugars can lead to damage in many parts of your child’s...
Mucopolysaccharidosis type II - MedlinePlus
Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a condition that affects many different parts of the body and occurs almost exclusively in men. Explore symptoms, inheritance, genetics of this condition.
MPS II (Hunter Syndrome) - Boston Children's Hospital
MPS II is also known as Hunter syndrome. Children with this condition have an abnormal accumulation of complex sugars in their cells, which affects many systems in their bodies. Hunter syndrome primarily occurs in boys and is one of about 50 diseases classified as lysosomal storage disorders (LSD).
Mucopolysaccharidosis Type II - GeneReviews® - NCBI Bookshelf
2007年11月6日 · Mucopolysaccharidosis type II (MPS II; also known as Hunter syndrome) is an X-linked multisystem disorder characterized by glycosaminoglycan (GAG) accumulation. The vast majority of affected individuals are male; on rare occasion …
Mucopolysaccharidosis Type II (MPS II) - Children's Hospital of ...
Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a rare inherited lysosomal storage disease in which the body is missing or does not have enough of an enzyme needed to break down long chains of sugar molecules called glycosaminoglycans (GAGs).
Mucopolysaccharidosis Type II - StatPearls - NCBI Bookshelf
2023年7月25日 · Mucopolysaccharidosis Type II (Hunter syndrome) is a rare X-linked recessive disorder. It has an early age of onset with clinical symptoms involving multiple organ systems. The severity of the disease depends on the phenotype. The …
Hunter Syndrome (MPS II): Causes, Symptoms, and Treatment
2024年12月4日 · What Is Hunter Syndrome (MPS II)? Hunter syndrome, also called mucopolysaccharidosis II or MPS II, is a rare disease that's passed on in families. It mainly affects boys. Their bodies can't...
Mucopolysaccharidosis type II (Hunter syndrome): a clinical …
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is a rare X-linked recessive disease caused by deficiency of the lysosomal enzyme iduronate-2-sulphatase, leading to progressive accumulation of glycosaminoglycans in nearly all cell types, tissues and organs.