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Regular noncompetitive physical exercise, however, is beneficial for Marfan patients. Good choices include brisk walking, shooting baskets, and slow-paced tennis.

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What effects can marfan syndrome have on a persons life?

They cant exercise as vigorously as someone without Marfan syndrome


What treatment is recommended for Marfan syndrome sufferers?

The treatment and management of Marfan is tailored to the specific symptoms of each patient. Some patients find that the syndrome has little impact on their overall lifestyle; others have found their lives centered on the disorder.


What portion of Marfan syndrome patients develop myopia?

Myopia (nearsightedness). Most patients with Marfan develop nearsightedness, usually in childhood.


How common is glaucoma among Marfan syndrome patients?

This condition is much more prevalent in patients with Marfan syndrome than in the general population.


Why are Marfan syndrome patients vulnerable to retinal detachment?

Retinal detachment. Patients with Marfan are more vulnerable to this disorder because of the weakness of their connective tissues.


What percentage of Marfan syndrome sufferers eventually develop cardiac complications?

About 90% of Marfan patients will develop cardiac complications.


How many Marfan syndrome sufferers develop ectopia lentis?

Between 50 and 80% of Marfan patients have dislocated lenses.


What evaluation should pregnant women with Marfan syndrome be given during each trimester?

It is recommended that patients have an echocardiogram during each of the three trimesters of pregnancy.


What happens to the dura membrane in Marfan syndrome patients?

The weak dura in Marfan patients swells or bulges under the pressure of the spinal fluid. This swelling is called ectasia.


Why should Marfan syndrome sufferers never smoke?

Smoking is particularly harmful for Marfan patients because it increases their risk of emphysema.


What cardiac monitoring is recommended for Marfan syndrome patients?

After a person has been diagnosed with Marfan, he or she should be monitored with an echocardiogram every six months until it is clear that the aorta is not growing larger. After that, the patient should have an echocardiogram once a year.


How can the chest of Marfan syndrome be deformed?

A few patients with Marfan may have a pectus excavatum on one side of their chest and a pectus carinatum on the other.