Hunter Syndrome Foundation

The Hunter Syndrome Foundation aims to fund and find a cure for Hunter Syndrome. Hunter Syndromeor Mucopolysaccharidosis Type II MPS IIis a rare genetic disorder that slowly destroys the bodys cells. This is a rare condition affecting 1 in 150,000 males.There is currently no cure, and the disease is progressive and life-limiting. The Hunter Syndrome

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The web site huntersyndromefoundation.org presently has an average traffic classification of zero (the lower the more users). We have analyzed four pages inside the web page huntersyndromefoundation.org and found seven websites interfacing with huntersyndromefoundation.org. There is one contacts and locations for huntersyndromefoundation.org to help you contact them. There is one public media sites linked to huntersyndromefoundation.org. The web site huntersyndromefoundation.org has been online for five hundred and fifty-four weeks, thirteen days, twenty-two hours, and sixteen minutes.
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The web site huntersyndromefoundation.org was first filed on November 23, 2013. It is now five hundred and fifty-four weeks, thirteen days, twenty-two hours, and sixteen minutes young.
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CONTACTS

Dancing with Dominic

E J Espinola

800 Willowmist Dr

Prosper, Texas, 75078

US

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Hunter Syndrome Foundation

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The Hunter Syndrome Foundation aims to fund and find a cure for Hunter Syndrome. Hunter Syndromeor Mucopolysaccharidosis Type II MPS IIis a rare genetic disorder that slowly destroys the bodys cells. This is a rare condition affecting 1 in 150,000 males.There is currently no cure, and the disease is progressive and life-limiting. The Hunter Syndrome

PARSED CONTENT

The web site has the following in the web site, "A CURE IS WITHIN REACH! Research for a Cure." I noticed that the web page also stated " What is Gene Therapy? The Hunter Syndrome Foundation aims to fund and find a cure for Hunter Syndrome." They also said " Hunter Syndrome or Mucopolysaccharidosis Type II MPS II is a rare genetic disorder that slowly destroys the bodys cells. This is a rare condition affecting 1 in 150,000 males. There is currently no cure, and the disease is progressive and life-limiting. One thought on Welcome! December 15, 2013 at 812 pm. Leave a Reply Cancel reply."

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