Lincoln’s likeness is everywhere, from the dime to the massive statue that dominates the National Mall in Washington, D.C.
Lincoln is interesting to historians because of his monumental role in American history during a time of great polarization, and he is fascinating to doctors because of his towering physical height.
A teenage Abraham Lincoln had a second mental collapse in January 1841. He passed out and was taken to a doctor who might have done more harm than good.
Lincoln suffered from depression beginning in his twenties and continuing throughout his life, according to historians.
Possible occurrences of Marfan syndrome have sparked a lot of interest. The attention that Marfan syndrome receives in Lincoln is sure to raise awareness of the condition among the general public and medical professionals, and it may even serve to offset a pervasive and regrettable attitude towards genetic sickness more generally.
Is Marfan Syndrome to Blame for Abe Lincoln’s Malformations?
The president’s unusually tall stature, his long, narrow face, and his gigantic hands and feet were the initial clues that Lincoln might have had Marfan syndrome.
Since it was first offered in the early 1960s, this concept has been hotly contested among geneticists and historians alike.
Because Marfan syndrome is a condition of the connective tissue, it has far-reaching effects on the body.
Abraham Lincoln may have suffered from this condition, which causes affected individuals to have extraordinarily lengthy limbs.
The Marfan Syndrome: What Is It?
Inherited in an autosomal dominant form or generated by de novo mutations, the prevalence of Marfan syndrome is estimated to be 2-2 per 10,000 people.
Connective tissue is affected by these alterations because fibrillin 1 is a protein found in the extracellular matrix.
The skeletal, visual, and cardiovascular systems are the primary sites of manifestation of this illness.
Overgrowth of long bones, long fingers, loose joints, dislocation of the ocular lens, early onset of myopia, and thickening of the heart valves that can cause mitral valve prolapse and varying degrees of valve regurgitation are all possible complications for patients.
Aortic aneurysm and dissection are the most lethal complications of Marfan syndrome; however, advances in diagnosis and treatment of these conditions have practically normalized life expectancy for those with the disorder.
How Long May Someone with Marfan Syndrome Expect to Live?
The syndrome is rather rare, with an incidence of 7-17,000 per 100,000. Without treatment, persons with Marfan syndrome have a 32-year life expectancy on average. Aortic dissection, aortic rupture, and heart failure from mitral and aortic valve regurgitation account for more than 90 percent of these deaths.
Do Persons Who Have Marfan Syndrome Have Any Chance of Leading a Typical Life?
Intricate and chronic, Marfan syndrome and its relatives are not to be taken lightly. Surgery, increased stress on bones and joints, and other issues owing to the diagnosis may all contribute to a long life expectancy, but they may not be pain-free.
In order to protect the heart from further damage, beta blockers are a common medication administered to people with Marfan syndrome.
An effective method of lowering blood pressure is using beta blockers (hypertension). However, the majority of those who suffer from Marfan syndrome also have hypotension (hypotension).