Mucopolysaccharidosis I (MPS I), pronounced mew-ko-pol-ee-sak-ah-ri-doh-sis one, is a rare genetic disorder that affects many body systems and that leads to organ damage. It is caused by a mutation in the gene that makes an enzyme called alpha-L-iduronidase (pronounced al-fa el eye-dur-on-i-dase).
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MPS I S, Scheie syndrome, is the mildest form of MPS I. Symptoms generally begin to appear after age 5, with diagnosis most commonly made after age 10. Children with Scheie syndrome have normal intelligence or may have mild learning disabilities; some may have psychiatric problems.
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/S), and Scheie syndrome (MPS I-S), listed from most to least severe.
Looking for online definition of MPS in the Medical Dictionary? MPS explanation free. What is MPS? Meaning of MPS medical term. What does MPS mean?
Mucopolysaccharidosis TYPE II (MPS II) is a serious genetic disorder that primarily affects males. It is one of several related lysosomal storage diseases. MPS interferes with the body’s ability to break down and recycle specific mucopolysaccharides (mew-ko-pol-ee-sak-ah-rides).
The Master of Professional Studies (MPS) is a master's degree that combines the focused study of traditional graduate degrees (such as the Master of Arts or Master of Science) with the specialized, industry-specific skills you can immediately put to use in the workplace.
What is MPS (Managed Print Services)? MPS is the consolidation and management of an organization’s copier and printer needs under a unified program, with equipment and service provided by an outside supplier, in our case, Ricoh.
MPS or Managed Print Services is a service offered by an external provider, Ricoh, to analyze and manage document output devices to reduce the total cost of ownership (including expenses for supplies, maintenance, and energy) and improve efficiency and productivity within the university. MPS includes:
MPS I disease is an inherited genetic disorder caused by a deficiency in an enzyme called alpha-L-iduronidase. Globally, MPS I occurs in about 1 in every 100,000 births.
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