MySheen

Pay close attention to Marfan syndrome to prevent bronchiectasis

Published: 2024-11-25 Author: mysheen
Last Updated: 2024/11/25, Marfan syndrome, also known as Marfan syndrome, is one of the hereditary connective tissues. Generally autosomal dominant inheritance, special physical performance, highlighting the chicken breast, limbs, fingers, toes are not symmetrical, height is obviously higher than the average person, companion.

Marfan syndrome, also known as Marfan syndrome, is one of the hereditary connective tissues. It is generally inherited by autosomal dominance, with special physical performance, prominent chicken chest, limbs, fingers and toes, slender asymmetry, height obviously exceeding ordinary people, accompanied by cardiovascular system abnormalities, especially combined heart valve abnormalities and aortic aneurysms. It may also affect other organs, including the lungs, eyes, dura mater, and hard jaw.

Here refers to Marfan syndrome is easy to cause bronchiectasis and other lung diseases, for infants with Marfan syndrome appearance or internal characteristics, we should pay close attention to its important attention and prevention of bronchiectasis, such as prevention of colds. Marfan syndrome is a congenital disease, so there is no perfect treatment for it, whether it is heart valve disease, aortic aneurysm disease or pulmonary bronchiectasis.

Marfan syndrome treatment and daily maintenance of various physiological disorders, available male hormones and vitamins, which are beneficial to collagen formation and growth. In addition, dominant different treatment is also different, Marfan syndrome shows congenital cardiovascular disease, suitable for early acute surgical repair, cardiac insufficiency, arrhythmia, suitable for medical treatment. If there is an aortic aneurysm or heart valve insufficiency, surgery should be considered as appropriate because drugs cannot remove the disease.

Because of the risk of ruptured aneurysms and bleeding, heart valve insufficiency also carries the risk of death from heart failure. Therefore, surgical treatment of Marfan syndrome, there are certain risks, should be different from person to person for a safe choice. However, with the advancement of science and technology, the success rate of surgery has been above 90%. If prompt has the aortic dissection aneurysm ruptures, should prompt the surgery treatment.

 
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