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5 Signs And Health Complications Linked To Marfan Syndrome

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By Author: Katerina Vlasova
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Marfan syndrome is a genetic disorder that affects the connective tissues in your body. These tissues help support and hold together organs, joints, and other important structures. When Marfan syndrome is present, these tissues are weaker than normal, which can lead to problems in many different areas of the body, including the heart, blood vessels, bones, eyes, and lungs.

This condition can range from mild to serious. Some people may only experience a few symptoms, while others may deal with life-threatening complications. Here are five important symptoms and health issues related to Marfan syndrome that you should know about.

1. Unusual Physical Features
One of the most visible signs of Marfan syndrome is how it affects the body’s shape and proportions. People with this condition are often very tall and thin. Their arms, legs, fingers, and toes may be longer than average and may appear out of proportion to the rest of the body.

Joint problems are also common. The joints may be overly flexible or unstable, which increases ...
... the risk of dislocations. Over time, the spine can start to curve abnormally, a condition known as scoliosis. The ribcage may also develop differently, causing the breastbone to either stick out or sink inward.

Facial features in people with Marfan syndrome are sometimes distinctive too. Their faces may appear long and narrow, and the roof of the mouth (palate) might be high and arched.

2. Problems With the Heart and Blood Vessels
Heart and circulatory problems are the most dangerous complications of Marfan syndrome. Because of this syndrome, the walls of your vessels may become weak and stretch significantly. This issue often affects the biggest artery (aorta) that ensures a blood supply from the heart to the rest of the body. When this artery stretches or weakens, it makes you prone to aortic aneurysm (aorta enlargement) and aortic dissection (tears in the inner layer).

Marfan syndrome often affects the heart valves. Because of weak connective tissues, the valves become floppy and cannot close tightly enough. This allows blood to leak backward to the artery. Mild leakage doesn't cause severe problems. But when the condition progresses, it causes excessive load on the heart and may contribute to heart failure. Marfan syndrome treatment can help preserve the health of your heart.

3. Dental and Jaw Issues
People with Marfan syndrome often have dental and jaw problems. Their jaws may be narrow, and their palates may be higher than normal. These changes can lead to crowded teeth, bite problems (like open bite or crossbite), and a higher chance of gum issues.

Because of the way their teeth and gums develop, people with Marfan syndrome may be more likely to have infections or other oral health concerns. They might also be at risk for temporomandibular joint (TMJ) disorders, which affect how the jaw moves and can cause pain.

Good oral hygiene and regular dental visits are very important. Dentists familiar with Marfan syndrome can provide care that helps prevent complications and maintain healthy teeth and gums.

4. Lung-Related Complications
Marfan syndrome can also impact the lungs. One of the most common problems is a collapsed lung (also called pneumothorax). This happens when air leaks into the space between the lung and the chest wall, causing the lung to collapse and leading to sudden chest pain and difficulty breathing.

Other possible lung problems include restrictive lung disease, where the lungs can’t expand fully. This can happen because of changes in the shape of the chest or spine. People with Marfan syndrome may also have a higher risk of developing conditions like asthma or emphysema, both of which can make breathing more difficult over time.

If you have Marfan syndrome and experience frequent shortness of breath, wheezing, or chest discomfort, it’s important to see a doctor. Lung problems can often be treated or managed with the right approach.

5. Vision and Eye Problems
Eye issues are common in people with Marfan syndrome. The most well-known problem is lens dislocation, which happens when the lens in the eye shifts out of place. This can lead to blurry vision or difficulty focusing.

Other common issues include an increased risk of retinal detachment, where the retina pulls away from the back of the eye. This can cause vision loss if not treated quickly. People with Marfan syndrome are also more likely to develop glaucoma (increased pressure in the eye) and cataracts (cloudy areas in the lens) at a younger age than most.

Regular eye exams are essential for monitoring and managing these problems. If caught early, many of these eye conditions can be treated effectively.

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