Abraham Lincoln
Lincoln dealt with severe depression and anxiety throughout his presidency. The issues were so problematic that it would cause him physical pain, such as headaches. But Lincoln turned to hobbies, such as storytelling and reading, to get him through his depression bouts.
Despite the impressive evidence of Marfan syndrome features in the president, Lincoln was not known to be loose-jointed, he was never known to have a heart murmur, there was no mention of aortic abnormalities at his autopsy, and he was not known to have the ocular abnormalities associated with Marfan syndrome [8,9].
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.
Marfan syndrome most commonly affects the heart, eyes, blood vessels and skeleton. People with Marfan syndrome are usually tall and thin with unusually long arms, legs, fingers and toes. The damage caused by Marfan syndrome can be mild or severe.
The expected lifespan of a person with Marfan syndrome used to be around the mid-40s age group, but now extends into the 70s – which is comparable to the general population. This improved lifespan is mainly due to: improved awareness of Marfan syndrome across health professionals.
Not all tall people have Marfan, but those who have it generally are much taller than average.
People with Marfan syndrome are often tall and thin, with very long arms, legs, fingers, and toes.
Interestingly, the final height of males with MFS is almost identical in different countries: 191.2±8.4 cm in France, 191.4±5.2 cm in Korea (9), and 191.3±9.0 cm (8) in the United States. This is true despite the difference in men's final height in each general population (174.4 vs.
Most people who have Marfan syndrome or a related condition are able to lead productive and satisfying lives, thanks to advances in medical treatment that have greatly extended life expectancy.
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 ...
Marfan syndrome (MFS) is a connective tissue disorder affecting the cardiovascular, ocular, and skeletal system, which may be accompanied by psychological features.
Although there is no cure for Marfan syndrome, doctors use treatments to relieve symptoms and prevent additional problems or complications. Treatment depends on the area of the body affected by the syndrome and may include: Medications to help manage pain and problems with your heart.
At a score of 175, Harvard grad John Quincy Adams has the highest estimated IQ of all U.S. presidents. He studied all around the world, becoming fluent in seven languages throughout his life.
Woodrow Wilson had dyslexia and struggled with reading his entire life. Instead of being overcome by his disability, Wilson used determination and self-discipline to not only survive in school, but to excel.
Lincoln knew that tensions were at an all-time high and needed to prioritize him and his family's safety. At this point, Lincoln is fully aware of his mental instability, particularly his depression and anxiety disorder (Schroeder-Lein 9-13). He has had many anxious episodes as well as depressing ones too.
Marfan syndrome does not affect intelligence.
Hopkins Medical Institutions, Baltimore, Maryland
We evaluated the neurodevelopmental status and cognitive ability of 30 school-age children with Marfan syndrome. We found average intellectual (mean full scale IQ = 109.3) and gross motor development.
Background: It is clinically widely overlooked that many patients with Marfan- (MFS) or Loeys-Dietz-Syndrome (LDS) are obese.
Marfan syndrome is a congenital condition, meaning a person has it from birth. Physical signs sometimes present in infancy but more often show up later in childhood or adolescence. Marfan syndrome affects approximately 200,000 people in the United States; both men and women of any race or ethnic group may be affected.
Children and young people may also display some behavioural and emotional problems and low self-esteem. They may suffer bullying or teasing at school if they have strong Marfanoid characteristics. They may additionally internalise their worries, resulting in withdrawal, physical complaints, anxiety and depression.
The Lujan-Fryns syndrome or X-linked mental retardation (XLMR) with marfanoid habitus syndrome is a syndromic X-linked form of intellectual disability, associated with tall, marfanoid stature, distinct facial dysmorphism and behavioral problems.
The reason why many people living with Marfan syndrome cannot gain weight isn't fully understood. It may have something to do with the underdeveloped muscles that are associated with Marfan syndrome.
The most common symptoms that lead to suspicion of MFS are external features and deviations noted during physical examination such as remarkably high stature, asthenic body structure, dolichostenomelia, arachnodactyly, chest deformities, characteristic facial attributes and other abnormalities.
If you have Marfan syndrome, you are at risk for a life-threatening problem in an important blood vessel in your chest called the aorta. If your aorta is weaker or larger than normal, it is important to know symptoms of a dissection, or rupture.