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3 studies found for:    Marfan Syndrome | Open Studies | NIH, U.S. Fed

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Rank Status Study
1 Unknown † Genetic Study of the FBN1 Gene and Fibrillin-1 Abnormalities in Choctaw Native Americans and Other Patients With Systemic Sclerosis
Condition: Systemic Sclerosis
Intervention:
2 Recruiting National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions
Conditions: Marfan Syndrome;   Turner Syndrome;   Ehlers-Danlos Syndrome;   Loeys-Dietz Syndrome;   FBN1, TGFBR1, TGFBR2, ACTA2 or MYH11 Genetic Mutation;   Bicuspid Aortic Valve Without Known Family History;   Bicuspid Aortic Valve With Family History;   Bicuspid Aortic Valve With Coarctation;   Familial Thoracic Aortic Aneurysm and Dissections;   Shprintzen-Goldberg Syndrome;   Other Aneurysms and Dissections of the Thoracic Aorta Not Due to Trauma, <50yo;   Other Congenital Heart Disease
Intervention:
3 Recruiting Clinical and Molecular Manifestations of Heritable Disorders of Connective Tissue
Conditions: Ehlers-Danlos Syndrome;   Stickler Syndrome;   Marfan Syndrome
Intervention:
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† Indicates status has not been verified in more than two years