Marfan syndrome(redirected from Marfan I syndrome)
Also found in: Medical.
A genetic disorder principally affecting the connective tissues of the body, manifested in varying degrees by excessive bone elongation and joint flexibility and by abnormalities of the eye and cardiovascular system.
[After Antonin Bernard Jean Marfan (1858-1942), French pediatrician.]
(Pathology) a disorder of connective tissue that is characterized by abnormal elongation of the bones and often by visual impairment
[C19: named after Antoine Marfan (1858–1942), French paediatrician]
Mar′fan syn`drome(ˈmɑr fæn, mɑrˈfæn)
a hereditary disorder characterized by abnormally elongated bones, hypermotility of the joints, and circulatory and eye abnormalities.
[after Antonin Bernard Marfan (1858–1942), French pediatrician, who described it in 1892]