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22 articles from the last 90 days matching "genetic disease"

ResearchCLINICALTRIALSMar 26

Trial Completed: Genetic Studies in the Amish and Mennonites (NCT00359580)

Researchers completed a study with 157 Amish and Mennonite participants to find the genes that cause inherited diseases common in these communities. They also created a family tree database using birth and marriage records to help understand how these genetic diseases run in families and what health problems develop over time.

WHY IT MATTERSThis completed research provides a genetic foundation for understanding rare inherited disorders in Amish and Mennonite populations, which could lead to earlier diagnosis and better treatment options for affected families in these communities.
Good to knowGenetic diseases in Amish populationsGenetic diseases in Mennonite populationsRead →
ResearchCLINICALTRIALSMar 26

Trial Now Recruiting: Human Biospecimen Procurement Protocol: Biorepository to Support Translational Research to Identify Disease Mechanism(s) (NCT02543996)

Researchers at the National Heart, Lung, and Blood Institute are collecting blood and tissue samples from up to 10,000 people to study rare genetic diseases. They want to understand what causes these diseases by examining the samples in a lab. People of any age with undiagnosed or heart and lung diseases can participate. Samples can be collected at the NIH Clinical Center or through your own doctor.

WHY IT MATTERSThis biorepository is actively recruiting and could help researchers identify the genetic causes of your undiagnosed condition, potentially leading to better treatments and diagnosis methods for rare diseases.
You can act on thisUndiagnosed DiseasesRare Genetic DiseasesCardiovascular DiseaseRead →
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