There is no cure, but treatments like enzyme replacement therapies can help make the disease more manageable. The sisters and maternal aunts of a person with MPS II may be carriers of the disease and would also have a 50 percent chance of passing the syndrome to a son. If the mother is a carrier, there is a 50 percent chance that any boy born will have the disease. Although rare, MPS II has been diagnosed in girls. MPS II primarily occurs in boys, and girls may be carriers of the gene for MPS II. This is a rare condition affecting 1 in 100,000 to 1 in 170,000 primarily males. Join MPS for a Young Learners Celebration Families with children ages 0-7 are invited to a fun back-to-school event Aug. Babies may show little sign of the disease, but as cells sustain damage, symptoms start to appear. These materials remain stored in the body’s cells, causing progressive damage. MPS II patients are missing the enzyme iduronate sulfatase, which is essential to breaking down the mucopolysaccharides dermatan and heparan sulphate. The body constantly replaces used materials and breaks them down for disposal. “saccharide” is a general term for a sugar molecule.“muco” refers to the thick jelly-like consistency of the molecules.Mucopolysaccharides are chains of sugar molecules used to build connective tissues in the body. MPS II has a wide range of symptoms that vary in severity and can be managed and treated with enzyme replacement therapies. It takes its name from Charles Hunter, the professor of medicine in Manitoba, Canada, who first described two brothers with the disease in 1917. MPS II is a mucopolysaccharide disease known as Hunter syndrome. 2022 National and Corporate Run/Walk Sponsors.I am always pleased to have feedback on my work on your behalf and on the web site so please feel free to get in touch. Upon login, you can view your CPD Records at-a-glance. ![]() Members of MPS will continue to access it for free. There are also details of how you can get in touch and when I hold my regular advice surgeries for which you do not need an appointment. With effect from 1st Jan 2021, the MPS CPDonline subscription rate shall be at RM127.20 ( RM120 + sst) per annum from 1st Jan - 31st Dec. Whilst I concentrate on housing, health and jobs, I speak on many other issues and the web site now provides a link to any speeches and any questions I ask in Parliament. Having campaigned for thorough Poynton flood prevention action plan, pleased this is now available on CheshireEast website. You can also access information on everything from the local campaigns I’m involved in, my voting record and the expenses I incur for my staff, travel and living during the week in London. My web site is designed to keep you up to date with what I am doing to represent the people of Stockton, Norton, Billingham, Stillington and the villages and includes links to social media as well as news about different activities. Much recent time has also been spent on fighting for the resources needed to combat increasing crime and anti social behaviour which is a major concern for local people following the massive Government cuts to policing budgets. That said, I continue to work in many different areas from NHS/health and social care to industry and carbon capture and storage, all topics which have a major impact on the area I represent. I look forward to working with the Shadow Justice Secretary, and the team, on building an effective criminal justice system. I was recently appointed as Shadow Minister for courts and sentencing. It is now over ten years since the people of Stockton North elected me to serve them in Parliament and I continue to do my best to do so.
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