What Famous Person Has Marfan Syndrome?

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.

Do basketball players have Marfan syndrome?

Isaiah Charles Austin

(born October 25, 1993) is an American former professional basketball player. He played two years of college basketball for Baylor University and was set to enter the NBA in 2014 until he was diagnosed with a mild form of Marfan syndrome.

What race is Marfan syndrome most common in?

Marfan syndrome affects men and women equally and occurs among

all races and ethnic groups

.

Who had marfans?

The 16th president of the United States,

Abraham Lincoln

, could be among one of the most famous people to have had Marfan syndrome.

Who was the first person with Marfan syndrome?

Can someone with Marfan syndrome gain weight?

Many people with Marfan syndrome have difficulty gaining weight, especially when they are younger

, no matter how much they eat and how many protein shakes they consume. Some do find that they do put on weight, particularly around their middle, when they get older.

Can Marfan skip a generation?

Approximately 25 percent of individuals who have Marfan syndrome, have the condition as a result of a new (de novo) mutation.

When a parent has Marfan syndrome, each of his or her children has a 50 percent chance (1 chance in 2) to inherit the FBN1 gene

.

How tall is the average person with Marfan syndrome?

Mean length at birth was 53 +/- 4.4 cm for males and 52.5 +/- 3.5 cm for females. Mean final height was

191.3 +/- 9 cm for males and 175.4 +/- 8.2 cm for females

.

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.

Are all Marfan patients tall?

The defective fibrillin gene also causes some bones to grow longer than they should. This means

a person with Marfan syndrome may be tall because their arms and legs grow longer than normal

. In the remaining quarter (25%) of cases, neither parent has the syndrome.

Does Marfan syndrome affect teeth?

Many people with Marfan syndrome and some related disorders have narrow jaws and high-arched palates, which can create dental and orthodontic problems

.

Does Michael Phelps suffer from Marfan syndrome?

In more recent times, Olympic swimmer Michael Phelps, basketball prospect Isaiah Austin and, perhaps, al-Qaeda leader Osama bin Laden had Marfan syndrome

.

What age is Marfan syndrome usually diagnosed?

Study Patients.

Their ages when the Marfan syndrome was first diagnosed ranged from

32 to 72 years

(mean age, 46 years). Of these 28 patients, 7 were older than 50 years of age at the time of initial diagnosis.

What can be mistaken for Marfan syndrome?

Examples of conditions that appear similar but have specific management are

Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome

.

What can Marfan be mistaken for?

Investigators say primary-care pediatricians and orthopedic surgeons should be on the lookout for Marfan-like features in all patients, but consider

Loeys-Dietz syndrome

if they also notice any of the following signs that are not found in Marfan: Widely spaced eyes. Club foot. Translucent skin that bruises easily.

Is Marfan syndrome a disability?

People who have Marfan syndrome are not able to qualify for SSDI benefits under an Social Security Administration (SSA) listing

. However, this does not mean that these individuals will be denied benefits. If complications of the condition are severe, these complications can qualify a person for benefits.

Can you go to the gym with Marfan syndrome?

The general guidelines for people with Marfan syndrome are to

avoid competitive and contact sports and enjoy recreational non-competitive sports and exercise

.

Should people with Marfan have children?

Pregnancy creates extra stress on the heart and blood vessels.

The biggest concern for patients with Marfan syndrome is serious complications of the aorta, such as a tear or rupture that can cause death or serious injury to both you and your unborn baby

. The risk is greatest if your aorta is dilated more than 4 cm.

Does Marfan syndrome affect the brain?

These vascular abnormalities can be a cause of cerebral and spinal ischemia or hemorrhage. Indeed,

ischemic events involving the brain or spinal cord are estimated to occur in 10% to 20% of patients with Marfan syndrome

.

Does Marfan syndrome affect the face?

Individuals with Marfan syndrome may have several distinct facial features including a long, narrow skull (dolichocephaly), deep-set eyes (enophthalmos), an abnormally small jaw (micrognathia) that may be recessed farther back than normal (retrognathia), abnormally flat cheek bones (malar hypoplasia), and an abnormal …

How tall are females with Marfan syndrome?

By contrast, the final height of females with MFS differs according to the country:

178.3±7.6 cm in France, 176.2±5.3 cm in Korea, and 175.4±8.2 cm in the United States

; in the general population, the final height in females is 162.5, 160.7, and 163.1 cm, respectively. The reason for this observation is unclear.

Can you have Marfan syndrome without heart problems?

About 90 percent of people diagnosed with Marfan syndrome will develop some type of problem with their heart or blood vessels

– most commonly affecting the aorta. However, once Marfan syndrome is diagnosed, treatment can address the risk of a serious heart problem.

What are 3 treatments for Marfan syndrome?

• Aortic repair. …
• Scoliosis treatment. …
• Breastbone corrections. …
• Eye surgeries.

Can you live a normal life with Marfan?

With access to modern medical management,

most people with Marfan syndrome have a normal life expectancy

. However;some people have died of the complications of Marfan syndrome. There is no cure for Marfan syndrome.

What is the quality of life for someone with Marfan syndrome?

To the Editor: Few studies have evaluated quality of life (QOL) in patients with Marfan syndrome (MFS). Most patients with MFS are

dissatisfied with their self-image, report low self-esteem, and express difficulty coping with the ramifications of their condition

.

What organs does Marfan syndrome affect?

Marfan syndrome is a genetic condition that affects connective tissue, which provides support for the body and organs. Marfan syndrome can damage the

blood vessels, heart, eyes, skin, lungs, and the bones of the hips, spine, feet, and rib cage

.

Can you drive with Marfan syndrome?

Marfan syndrome and other inherited aortopathies

✓-

May drive and need not notify DVLA if no aneurysm

. ✘- If there is an aortic aneurysm must notify DVLA and must not drive if the aortic diameter exceeds 5cm.

Does Marfan syndrome cause headaches?

People with Marfan syndrome are at particular risk of developing dural ectasia. As the membrane expands, it can press on the vertebrae in your lower back, which can cause:

backache

.

headache

.

Is Marfan syndrome fatal?

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.

Does Osama bin Laden have Marfan syndrome?

At the time of 9/11, bin Laden was very ill.

He is believed to have had Marfan syndrome

, a degenerative genetic disorder that shortens life-spans and makes sufferers unusually tall with long limbs and narrow fingers.

Does Marfan syndrome cause joint pain?

They raise your blood pressure and heart rate, which may increase the risk of an aortic tear. These activities also place a strain on your joints.

As people with Marfan syndrome often have weak joints, their risk of sustaining a joint injury during these activities may be increased

.

Can you exercise with Marfan syndrome?

In general,

most people living with Marfan syndrome should exercise regularly through low-intensity (aerobic), low-impact activities adapted to meet their specific needs

. Nearly every activity can be done at different intensity levels, and no recommendation holds true in all circumstances.

What is the average height of someone with Marfan syndrome?

Mean length at birth was 53 +/- 4.4 cm for males and 52.5 +/- 3.5 cm for females. Mean final height was

191.3 +/- 9 cm for males and 175.4 +/- 8.2 cm for females

.

What is the life expectancy of someone with Marfan?

The prevalence of the syndrome is 7-17/100,000. 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.

What percent of the population has Marfan syndrome?

Marfan syndrome is rare, happening in about

1 in 5,000 people

. Marfan syndrome is caused by a mutation in a gene called FBN1. The mutation limits the body’s ability to make proteins needed to build connective tissue. One in four people with Marfan syndrome develops the condition for unknown reasons.