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Marfan Europe Network: Together we can!
Margit Aschenbrenner1,2, Tuija Ekegren1,3, Françoise Steinbach1,4
1Marfan Europe Network.
FEBS Letters
|October 10, 2025
Summary
Marfan syndrome is a rare genetic connective tissue disorder. The Marfan Europe Network (M.E.N.) connects patients and organizations to improve lives and public awareness.
Area of Science:
- Genetics
- Medicine
- Rare Diseases
Background:
- Marfan syndrome, a rare genetic disorder, affects connective tissue.
- Caused by FBN1 gene mutations, it presents with variable phenotypes including tall stature, joint hypermobility, eye issues, and aortic enlargement.
- While treatable, patient education and support are crucial.
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