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Marfan syndrome (MFS) is a rare genetic disease (1/5000) characterized by the association of ocular impairment, cardiovascular disease and musculoskeletal disease. In some chronic conditions, physica...
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Lead Sponsor
University Hospital, Toulouse
NCT04194619 · Vascular Anomaly, Osler Rendu Disease, and more
NCT05838235 · Marfan Syndrome
NCT05702476 · Rare Diseases, Marfan Syndrome
NCT05809323 · Marfan Syndrome
NCT05123339 · Marfan Syndrome
CHU de Toulouse
Toulouse, Midi-Pyrénées
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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