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What is Hunter syndrome? Also known as MPS II


This video provides an overview of Hunter syndrome, or mucopolysaccharidosis II (MPS II) -- a serious genetic disorder that primarily affects males. In Hunter ...
 

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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 ...
 

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Meet the siblings who have Hunter's Syndrome


The Hunter's Syndrome is considered as one of the rare diseases. The price needed to cure this disease is estimated to be at half a million pesos. Here in the ...
 

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Hunter Syndrome Awareness


Finding an underlying cause to your child's long list of childhood illnesses and repeat visits to your pediatrician can be tough. But it'll also be a huge relief when ...
 

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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, ...
 

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Understanding Hunter syndrome (MPS II)


This short video is about Hunter syndrome, or mucopolysaccharidosis II (MPS II), a serious genetic disorder that primarily affects males. It interferes with the ...
 

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The progression of Hunter syndrome (Long Version)


Hunter syndrome is a progressive disease, meaning signs and symptoms develop over time. This video outlines the signs and symptoms of Hunter syndrome ...
 

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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 ...
 

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I-Witness (March 05,2012) hunter syndrome


para sa mga gustong tumulong visit \
 

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Early signs and symptoms of Hunter syndrome


This short video describes the early symptoms of Hunter syndrome (MPS II). Symptoms are generally not apparent at birth, but usually start to become noticeable ...
 

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Will - Hunter Syndrome


Will has Hunter Syndrome.
 

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Hunter Syndrome


A video I made of these amazing kids with Hunter Syndrome!
 

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Raising Rare Boys - Cure Hunter Syndrome


Hunter Syndrome occurs in 1 in 100000 male births. It's very rare, there is no cure and no treatment that affects the brain and improves cognitive function.
 

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Tunay na Buhay: Tatlong magkakapatid, lumalaban sa parehong karamdaman


Aired: September 21, 2016 Ang Hunter's Syndrome ay isang hindi pangkaraniwang kondisyon na tumatama lamang sa 200 Pilipino. Bibisitahin ni Rhea Santos ...
 

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hunter syndrome phil.


 

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Hunter Syndrome - Mucopolysaccharidosis II PSA


Created using PowToon -- Free sign up at http://www.powtoon.com/youtube/ -- Create animated videos and animated presentations for free. PowToon is a free ...
 

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Understanding Hunter and Hurler Syndrome


Steven L. Schoenfeld, MD, vice president, clinical affairs at AmeraGen discusses the pathophysiologies of Hunter and Hurler syndromes and how both ...
 

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Mission Possible: Vice Ganda surprises brothers with Hunter Syndrome


Watch as Vice Ganda surprises his fans, the Parco brothers. The 3 brothers have a rare disease called Hunter Syndrome. Subscribe to the ABS-CBN News ...
 

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hunter syndrome YouTube 948ad7e81bc374b6


sa mga gustong tumulong visit: www.psod.org.ph.
 

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We recently spoke with Marielle, a parent of a child with MPS II (Hunter syndrome). She describes what Hunter syndrome is, her and her husband's initial ...
 

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Diagnosing Hunter Syndrome - ENT Doctors May Be the First to Spot MPS II


Dr. David E. Karas, MD, a pediatric otolaryngologist at the Yale-New Haven Hospital, discusses the key role ENTs play in the diagnosis of syndromes like MPS II.
 

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Story of a chid who suffered from inherited genetic disorder \


A five years child Shaurya is suffering for rare disease \
 

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MPS-II (Hunter Syndrome) Zwillinge aus Weiden in der Oberpfalz


10.03.2012: Wieder vereint!*** ***2010: In den frühen Morgenstunden des 11.September 2010 schlief Jannic nach grossem und tapferem Kampf für immer ein.
 

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An interview on Hunter syndrome (MPS II) with Dr John Mitchell


This video features an interview with Dr John Mitchell. An interview on Hunter syndrome (MPS II) with Dr John Mitchell In this interview, Dr John Mitchell talks ...
 

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Having a brother with Hunter Syndrome


 

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Key Features of Hunter syndrome: MPS II Global Webinar - Part 1


Hunter syndrome (MPS II) is a lysosomal storage disorder. The disease is caused by a genetic defect but is also an active process and so the signs and ...
 

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hunter syndrome Medium


The information in this video was retrieved from the following sources: American Speech-Language-Hearing Association. (2008).Roles and responsibilities of ...
 

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KRPIA Patient Video Hunter Syndrome


 

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MPS II Global Webinar - Part 2: Multisystemic Manifestations of Hunter syndrome


Hunter syndrome (MPS II) is a heterogeneous disease with multisystemic and multiorgan involvement; each patient will have a unique presentation and the ...
 

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The progression of Hunter syndrome (Short Version)


Hunter syndrome is a progressive disease, meaning signs and symptoms develop over time. This short video outlines the signs and symptoms of Hunter ...
 

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Additional signs and symptoms of Hunter syndrome


This short video shows how Hunter Syndrome signs and symptoms emerge over times. These symptoms may include cardiac/valvular heart disease, short ...
 

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The Balancing Act – Hunter syndrome – Part 2 of 2


Hunter syndrome, or mucopolysaccharidosis II (MPS II), is a serious rare genetic disorder that primarily affects males. This video features a conversation with ...
 

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Multisystemic Manifestations of Hunter syndrome: MPS II Global Webinar - Part 2


Hunter syndrome (MPS II) is a heterogeneous disease with multisystemic and multiorgan involvement; each patient will have a unique presentation and the ...
 

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The Balancing Act – Hunter syndrome – Part 1 of 2


Hunter syndrome, or mucopolysaccharidosis II (MPS II), is a serious rare genetic disorder that primarily affects males. This video features a discussion about the ...
 

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Steve Nash and Simon Ibell on Hunter Syndrome


Steve Nash and Simon Ibell ask that Enzyme Replacement Therapy be funded by the Provincial Ministries of Health. To sign the petition go to: ...
 




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