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Prader-Willi Syndrome (PWS) is a genetic disorder that occurs in approximately one out of every 15,000 births. PWS is recognized as a common genetic cause of childhood obesity. Currently there is no cure for PWS.
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Neurofibromatosis (NF) is an umbrella name for 3 distinct complex genetic disorders that share a common manifestation: tumour growth in the tissues that surround nerves producing skin and bone abnormalities.
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Cryopyrin-Associated Periodic Syndromes are a very rare set of disorders, there are fewer than 1000 cases of CAPS have been reported in the world, but more than 5500 people may actually have CAPS and not know it.
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CORD
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Do if for future gen...
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12.22.2010
- Goal:
$500
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HAE Canada
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HAE Canada Virtual W...
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05.08.2013
- Goal:
$600
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