If you are suffering from a severe case of Marfan syndrome and it has made you unable to work, you may be eligible to
Social Security disability benefits
. While people from all around the world, of all races and genders, can suffer from Marfan syndrome, the symptoms of the condition have a tendency to worsen with age.
Do people with Marfan syndrome have learning disabilities?
The syndrome affects different people in different ways, but
Marfan syndrome does not cause learning disabilities
. People with Marfan may: be taller than normal. have a lean, lanky build, as well as long, thin fingers and toes.
Is Marfan syndrome a mental illness?
Introduction. Marfan Syndrome (MFS),
a disease of microfibril dysfunction
, has been associated with schizophrenia in multiple case reports.
Is Marfan syndrome a terminal illness?
How often is the condition fatal?
Marfan’s disease used to always be fatal
—a person wouldn’t normally live past the age of 45. Today, with aggressive treatment, people can live well beyond that. One of the difficulties is that in patients with Marfan’s disease you tend to chase the aorta.
How serious is Marfan syndrome?
Marfan syndrome can
damage the blood vessels, heart, eyes, skin, lungs, and the bones
of the hips, spine, feet, and rib cage. Some complications of Marfan syndrome can be treated or prevented, including heart disease, bone deformities such as a curved spine, eye conditions, crooked teeth, and collapsed lungs.
What famous person has Marfan syndrome?
Abraham Lincoln
is the most famous American who had Marfan syndrome. So did Julius Caesar and Tutankhamen. In more recent times, Olympic swimmer Michael Phelps, basketball prospect Isaiah Austin and, perhaps, al-Qaeda leader Osama bin Laden had Marfan syndrome.
Does Marfan syndrome shorten your life?
One in 10 patients may have a high risk of death with this syndrome due to heart problems. Despite the high risk for Marfan related cardiovascular problems, the average life expectancy of those with Marfan syndrome is
nearly 70 years
. The life expectancy in this syndrome has increased to greater than 25% since 1972.
Can you have marfans and not be tall?
How Do Doctors Diagnose It?
Not everyone who’s tall or thin or nearsighted has the disease
. People who have Marfan syndrome have very specific symptoms that usually occur together, and it’s this pattern that doctors look for when diagnosing it.
What race is Marfan syndrome most common in?
Marfan syndrome affects men and women equally and occurs
among all races and ethnic groups
. Because it’s a genetic condition, the greatest risk factor for Marfan syndrome is having a parent with the disorder.
Does Marfan syndrome get worse with age?
Marfan syndrome can be mild to severe, and
may become worse with age
, depending on which area is affected and to what degree. In Marfan syndrome, the heart is often affected. The aorta, the major artery of the body, may be more dilated (widened) than average.
What is the life expectancy of someone with Marfan?
The mean life expectancy for untreated patients with Marfan syndrome
is 32 years
with aortic dissection, aortic rupture or cardiac failure due to mitral and aortic valve regurgitation as the predominant cause of death in > 90% of the cases.
Does Marfan syndrome affect teeth?
Many people with Marfan syndrome have narrow jaws and a high-arched palate, which can create dental (tooth) and orthodontic (alignment) problems.
What age is Marfan syndrome usually diagnosed?
We found a median age at
diagnose of 19.0 years
(range: 0.0–74). The age at diagnosis increased during the study period, uninfluenced by the changes in diagnostic criteria.
Can you have Marfan syndrome without heart problems?
Even though heart and blood vessel problems affect about 9 out of every 10 people diagnosed with Marfan syndrome, there is good news. If you get diagnosed, you have a lot of options, including having surgery, taking medications and changing your physical activities.
What is the difference between Marfan and Ehlers Danlos?
Unlike Marfan syndrome,
the fragile tissues and skin and unstable joints found
in Ehlers-Danlos syndrome are due to defects in a group of proteins called collagen, proteins that add strength and elasticity to connective tissue.
Can you play sports with Marfan syndrome?
Participation in competitive athletics for the individual with
Marfan syndrome is prohibited except for low intensity sports such as golf, bowling, and others not associated with intense physical exertion and bodily collision
as outlined in the 36th Bethesda Conference
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This recommendation is based on the concern that …
