Marfan Syndrome Market Intelligence: Key Insights and Growth Trends
Marfan syndrome is a rare genetic disorder that affects connective tissue, impacting multiple organs, including the heart, blood vessels, bones, and eyes. It is caused by a mutation in the fibrillin-1 (FBN1) gene, which weakens connective tissue structures. As an autosomal dominant condition, it can be inherited from an affected parent.   Despite its...
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