Lincoln is thought to have had Marfan's disease. what is it

Marfan syndrome is a genetic disorder that affects the connective tissue. Connective tissue is what holds the body together, so it can affect many different parts of the body, including the heart, blood vessels, bones, and eyes.
People with Marfan syndrome are typically tall and thin, with long arms and legs, and a narrow chest. They may also have a high arched palate, scoliosis, and loose joints.
The most serious complications of Marfan syndrome are related to the heart and blood vessels. The aorta, the main artery that carries blood from the heart to the rest of the body, can enlarge and rupture. This can be a life-threatening condition.
Other complications of Marfan syndrome can include:
- Mitral valve prolapse, a condition in which the mitral valve in the heart does not close properly
- Dislocation of the lens of the eye
- Retinal detachment
- Pneumothorax, a collapsed lung
There is no cure for Marfan syndrome, but there are treatments that can help to manage the symptoms and prevent complications. These treatments may include:
- Medications to control blood pressure and heart rate
- Surgery to repair or replace the aorta
- Eyeglasses or surgery to correct vision problems
People with Marfan syndrome should be monitored regularly by a healthcare team that includes a cardiologist, an ophthalmologist, and a geneticist. With early diagnosis and treatment, people with Marfan syndrome can live long and healthy lives.
The diagnosis of Marfan syndrome is based on a combination of physical examination, family history, and genetic testing. There is no single test that can definitively diagnose Marfan syndrome, so doctors will look for a cluster of characteristic features.
If you are concerned that you or your child may have Marfan syndrome, talk to your doctor. They can help you to get the necessary testing and treatment.
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