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- Mucopolysaccharidosis type I (MPS I) is a rare disease in which the body is missing or does not have enough of an enzyme ... to a group of diseases called mucopolysaccharidoses (MPSs). MPS I is the most common. There are several ...
- Mucopolysaccharidosis type III (MPS III) is a rare disease in which the body is missing or does not have enough of certain enzymes ...
- Mucopolysaccharidosis type IV (MPS IV) is a rare disease in which the body is missing or does not have enough of an enzyme ... to a group of diseases called mucopolysaccharidoses (MPSs). MPS IV is also known as Morquio syndrome. There ...
- Mucopolysaccharidosis type II (MPS II) is a rare disease in which the body is missing or does not have enough of an enzyme ... to a group of diseases called mucopolysaccharidoses (MPSs). MPS II is also known as Hunter syndrome. There ...
- Mucopolysaccharidosis type I (MPS I) is a condition that affects many parts of the body. This disorder was once divided into three separate syndromes: Hurler syndrome (MPS I-H), Hurler-Scheie syndrome (MPS I-H/ ...
- ... problems. There are several types of MPSs, including: MPS I (Hurler syndrome; Hurler-Scheie syndrome; Scheie syndrome) MPS II (Hunter syndrome) MPS III (Sanfilippo syndrome) MPS ...
- MPS Diseases (National MPS Society)What is MPS? Learn more about rare diseases including Sanfilippo syndrome, Hunter syndrome, and Hurler syndrome
- Mucopolysaccharidosis type IV (MPS IV), also known as Morquio syndrome, is a progressive condition that mainly affects the skeleton. The rate at which ... affected individuals.The first signs and symptoms of MPS IV usually become apparent during early childhood. Affected ...
- ... cytochrome P-450MP cytochrome P450 2C9 cytochrome P450 MP-4 cytochrome P450 MP-8 cytochrome P450 PB-1 cytochrome P450, family ... family 2, subfamily C, polypeptide 9 gene P450 MP-4 S-mephenytoin 4-hydroxylase S-mephenytoin 4- ...
- Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a condition that affects many different parts of the body. The condition ... varies among affected individuals.At birth, individuals with MPS II do not display any features of the ...