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Marfan syndrome
(redirected from Marfans)

   Also found in: Dictionary/thesaurus, Medical, Wikipedia 0.03 sec.

Marfan syndrome

Rare hereditary disorder of connective tissue. Affected persons are tall, with long, thin limbs and spiderlike fingers (arachnodactyly). The lens of the eye is dislocated, and many have glaucoma or detached retina. Heart muscle abnormalities and various malfunctions and malformations occur; rupture of the aorta is the most common cause of death. Severity varies; affected individuals may die young or live essentially normal lives. The underlying abnormality cannot be cured, but some of the defects can be surgically corrected.



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They revealed the former Haybridge High School pupil, who was nicknamed Dime, had Marfans syndrome.
Her son Stuart died seven years ago aged 20 after battling Marfans Syndrome and the family have been fundraising for the Marfans Association.
Family requests donations be made to the National Marfans Foundation, 22 Manhasset Avenue, Port Washington, New York 11050.
 
 
 
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