Neonatal Progeroid Foundation
NPS is an extremely rare aging syndrome. Help us bring educate, bring awareness and fundraise!.. Neonatal Progeroid Foundation 501c3 was created to bring awareness to Neonatal Progeroid Syndrome (NPS), previously named Wiedemann Rautenstrauch Syndrome. Through recent research, we have learned that the syndrome occurs when there are two mutations on the PolR3A gene. We are thankful for the doctors who have helped us gain more insight on NPS, but are looking for doctors to help us find treatments. Due to NPS being extremely rare, finding any help will almost completely come from donations and this is why Neonatal Progeroid Foundation was created.
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Birth Defects, Genetic Diseases Research Category
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