Loeys-Dietz Syndrome Foundation
The LDSF is a 501(c)3 non-profit organization organization dedicated to:--encouraging education about Loeys-Dietz syndrome and related connective tissue disorders to medical professionals and lay communities in order to aid in identification, diagnosis and treatment of Loeys-Dietz syndrome--fostering research about Loeys-Dietz syndrome--providing a support network, for individuals, parents and families affected by Loeys-Dietz syndrome
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Loeys-Dietz Syndrome Foundation This March were celebrating 20 years since LoeysDietz Syndrome was first identified. Join us as we raise awareness share stories and support those affected. Together we honor two decades of progress and continue advocating for the LDS community. Our purpose is to provide information about what LoeysDietz syndrome LDS is and to provide hope for those impacted by the condition.
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