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 …
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.
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.
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).
Hunter Syndrome (MPS II): Causes, Symptoms, and Treatment - WebMD
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...
Mucopolysaccharidoses | National Institute of Neurological …
2024年7月19日 · MPS II (also known as Hunter syndrome) is caused by a lack of the enzyme iduronate-2-sulfatase. MPS II is the only mucopolysaccharidosis disorder in which inheriting a single defective gene from the mother can result in mucopolysaccharidosis in a son (called X-linked recessive inheritance).
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 - 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 …
Mucopolysaccharidosis type II | Newborn Screening
There are two main types of MPS II – the severe type and the attenuated type – that differ in signs, symptoms, and age of onset. The severity of the condition depends on how much I2S activity is present in the body.
MPS II (Hunter Syndrome) - Boston Children's Hospital
What is MPS II (Hunter syndrome)? Mucopolysarcharidosis type II (MPS II) is a rare, inherited disorder. 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 …