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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.
Hunter syndrome is a rare genetic disorder in which your child’s body doesn’t properly break down (digest) certain sugar molecules. When these molecules build up in organs and tissues over time, they can cause damage that affects physical and mental development. Healthcare providers classify Hunter syndrome into severe and mild types.
May 1, 2024 · Hunter syndrome is a inherited genetic disorder that leads to the build-up of a sugar called GAGs that can lead to damage in many parts of your child’s body.
Jul 25, 2023 · 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 severe phenotype has high morbidity and mortality.
What is Hunter syndrome? Hunter syndrome (also called mucopolysaccharidosis, type 2 or MPS II) is a genetic condition in which the body creates too little iduronate 2-sulfatase enzyme (an enzyme that helps the body break down certain types of sugar). Hunter syndrome typically affects biological males (people assigned male at birth).
Jul 25, 2023 · Hunter syndrome is when someone is born with a specific digestive enzyme deficiency called lysosomal enzyme iduronate-2-sulfatase deficiency. Hunter syndrome prevents the breakdown of sugars leading to the buildup of complex sugars called glycosaminoglycans (GAGs).
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 their bodies.
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), 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, or mucopolysaccharidosis II (MPS II), is a rare, X-linked, recessive disorder that almost exclusively affects males. This website is a resource for people with Hunter syndrome (MPS II), their family and friends.
