Das Marfan-Syndrom ist eine lebensbedrohliche genetisch bedingte Erkrankung des Bindegewebes. Wenn die Anzeichen des Marfan-Syndroms richtig erkannt werden, eine korrekte Diagnose gestellt wird und die Erkrankung richtig behandelt wird, können Patienten mit Marfan-Syndrom ein langes und erfülltes Leben führen.
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Shprintzen-Goldberg Syndrome Fact Sheet
Shprintzen-Goldberg Syndrome is a condition that affects many parts of the body. People who have this syndrome have a combination of unique facial features and skeletal and neurological abnormalities. Shprintzen-Goldberg syndrome is caused by genetic changes (mutations) in a gene that contributes to the formation of connective tissue. How prevalent is Shprintzen-Goldberg syndrome? What are […]
Directives Relatives à L’activité Physique
La pratique régulière d’activités physiques améliore tant le bien-être physique que psychologique et peut s’intégrer en toute sécurité aux habitudes des personnes atteintes du syndrome de Marfan. Ces personnes sont par conséquent encouragées à adapter les mesures sanitaires qui les protègent des caractéristiques de Marfan qui pourraient s’aggraver et des affections qui font simplement partie […]
Tags: Marfan Syndrome , Patients & Families
Genetic Testing and Marfan Syndrome
Genetic testing for mutations in fibrillin-1 (FBN1) and other genes has become an important and reliable option to aid in the diagnosis of Marfan syndrome and related disorders. However, the results of genetic testing for the diagnosis of disorders are not always straightforward. Therefore, working with a medical geneticist (a physician with training in genetics) […]
Tags: Marfan Syndrome , Patients & Families
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