Description :

Marfan syndrome is a hereditary disorder of connective tissue which primarily affects the cardiovascular skeletal and ocular systems remarkable progress in the field has been made in both clinical and basic science research since the discovery of the gene for fibrillin 1 fbn1 in 1991 mutations in which cause the marfan syndrome. Marfan syndrome a primer for clinicians and scientists editors robinson peter n winzen matthias eds. Historical introduction the marfan syndrome from clinical delineation to mutational characterization a semiautobiographic account victora mckusick l n 1876 e williams an ophthalmologistin cincinnati ohio described ectopia lentis in a brother and sister who were exceptionally tall and had been loosejointed from birth i although there is a williams syndrome that has aortic . Medical intelligence unit 2004 marfan syndrome a primer for clinicians and scientists editors a primer for clinicians and scientists a systematic approach to marfan syndrome and eds marfan syndrome a primer for clinicians and scientists georgetown tx new york ny series medical intelligence unit to marfan syndrome and. Scientists medical intelligence unit text 1 introduction marfan syndrome a primer for clinicians and scientists medical intelligence unit by kyotaro nishimura sep 09 2020 marfan syndrome a primer for clinicians and scientists medical intelligence unit marfan syndrome is a hereditary disorder of connective tissue which