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HunterSyndrome news

'We actually could save these kids': Mom raises money to cure rare disease


Today.com - Dec 28, 2017
Last year, the Muedder family discovered that their then 2-year-old son Finn has Hunter syndrome, a rare genetic disease with a terrible prognosis — children with it slowly lose their ability to walk, talk, and eat, and most die as teenagers. Almost ...
 

Headline-grabbing attempt to edit living human's DNA needs reality check


Genetic Literacy Project - Jan 22, 2018
Sangamo also is working on another metabolic disorder, Hurler syndrome (a disease in the same category as Hunter syndrome) and two types of hemophilia, Factor VIII deficiency (classical hemophilia) and Factor IX deficiency (Christmas disease). If those ...
 

Mucopolysaccharidosis II {MPS II} {Hunter Syndrome } – Pipeline Review |Therapeutics Development by Leading Key ...


Medgadget (blog) - Jan 11, 2018
A new independent 53 page research with title 'Mucopolysaccharidosis II {MPS II} {Hunter Syndrome } – Pipeline Review, H2 2017' guarantees you will remain better informed than your competition. The study covers geographic analysis that includes ...
 

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What Is Hunter Syndrome?


For more information, visit: http://projectalive.org Video Produced by Caravan: http://wearecaravan.tv.
 

What is Hunter Syndrome?


Parents Chris and Melissa and The Doctors are joined by Hunter Syndrome expert Dr. Patricia Dickson to talk about this rare condition. And their son Case joins the stage to receive some very...
 

What is Hunter Syndrome?


Hunter syndrome (MPS II) is a hereditary disease. It is a lysosomal storage disorder caused by the deficiency or absence of the lysosomal enzyme iduronate-2-sulfatase. The deficiency or absence...
 

First human clinical trial for Hunter syndrome underway at Emory


A first-in-man clinical trial, testing a newly developed drug for a rare genetic condition called mucopolysaccharidosis type II (MPS II) or Hunter syndrome, is underway at Emory University.
 

Another PGD story: Hunter syndrome


Kendra Lesta tells Norah O'Donnell about losing her son Christopher to a rare disease and why she did PGD to prevent passing it on again. Watch Norah O'Donnell's full report: http://cbsn.ws/1zdkwQM.