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).
Available immediately from VitalStream's direct sales team, the MediaConsole MPS solution will be demonstrated for the first time during NAB 2005, Las Vegas, NV at VitalStream's Booth #SL1023 and at thePlatform's booth #SL3322.
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MPS I H (also called Hurler syndrome or α-L-iduronidase deficiency), is the most severe of the MPS I subtypes. Developmental delay is evident by the end of the first year, and patients usually stop developing between ages 2 and 4.
Mucopolysaccharidosis I (MPS I) is a rare genetic disorder that affects both physical and mental development and can cause organ damage.
What Is MPS 2? Mucopolysaccharidosis 2 (mew-ko-pol-ee-sak-ah-ride-osis). Mucopolysaccharidosis TYPE II (MPS II) is a serious genetic disorder that primarily affects males.
The MPS offering is currently available in the MPS v2 2000 plan only. Verio Unveils Industry's First IPv4/v6 Dual Stack Virtual Private Server Hosting Solution Films Media Group is one of the latest customers to select MPS .
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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.
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