Tag: Hunter Syndrome
Mucopolysaccharidosis Type II
Mucopolysaccharidosis Type II: Definition and Description of Mucopolysaccharidosis Type II: Mucopolysaccharidosis Type II (MPS II), also known as Hunter syndrome, is a rare genetic disorder that falls under the category of lysosomal storage diseases. It is caused by a deficiency of the enzyme iduronate-2-sulfatase (I2S), which plays a crucial role in breaking down glycosaminoglycans (GAGs).…
MPS Disorder II
MPS Disorder II: Definition and Description of MPS Disorder II: MPS Disorder II, also known as Hunter Syndrome, is a rare genetic disorder that affects the body’s ability to break down certain types of carbohydrates known as glycosaminoglycans (GAGs). This condition is caused by a deficiency in the enzyme iduronate-2-sulfatase, which leads to the accumulation…
MPS II
MPS II: Definition and Description of MPS II: MPS II, also known as Hunter syndrome, is a rare genetic disorder categorized under mucopolysaccharidosis. It arises from a deficiency of the enzyme iduronate-2-sulfatase (I2S), which is critical for the breakdown of glycosaminoglycans (GAGs). This enzyme deficiency leads to an accumulation of GAGs in various tissues and…
Mucopolysaccharidoses
Mucopolysaccharidoses: Definition and Description of Mucopolysaccharidoses: Mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders caused by the deficiency of specific enzymes necessary to break down glycosaminoglycans (GAGs), which are long chains of sugar molecules. These enzymes play a vital role in metabolism, and their deficiency leads to the accumulation of GAGs in various…
Hunter Syndrome
Hunter Syndrome Definition and Description of Hunter Syndrome Hunter Syndrome, also known as mucopolysaccharidosis type II (MPS II), is a rare genetic disorder that primarily affects males. It is caused by the deficiency of an enzyme called iduronate-2-sulfatase, which is essential for the breakdown of complex carbohydrates known as glycosaminoglycans (GAGs). When this enzyme is…