Category: Genetic Disorders / Connective Tissue Disorders
Marfan Syndrome is a systemic disorder of connective tissue caused by a mutation in the FBN1 gene, primarily affecting the skeletal, ocular, and cardiovascular systems, leading to features like tall stature, lens dislocation, and aortic aneurysm.
Estimated at 1 in 5,000 to 1 in 10,000 people worldwide (Source: National Marfan Foundation).
Discover the latest clinical trials and treatments for Marfan Syndrome (Detailed) on JourneyForHealth.
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