How to treat Marfan syndrome

summary

Marfan syndrome is an autosomal dominant hereditary disease with connective tissue as the basic defect. Next, let's talk about the symptoms of this disease, and hope you can prevent it early.

How to treat Marfan syndrome

Symptom 1: autosomal dominant hereditary disease with basic defect, involving bone, eye and cardiovascular system, without affecting intellectual development.

Symptom 2: the clinical typical skeletal system changes are tall and thin, the upper body is shorter than the lower body, the distal part of the limbs is slender, forming spider foot like fingers (toes), often flat chest, pectus excavatum, thoracic kyphosis or scoliosis;

Symptom 3: high myopia, lens dislocation or subluxation are the main manifestations of the eyes; the patients have dissecting aortic aneurysm or aortic aneurysm like dilatation with aortic valve insufficiency due to cystic necrosis in the middle layer of the ascending aorta, and some patients still have the manifestations of mitral valve mucoid degeneration and mitral valve prolapse.

matters needing attention

Once you find the above symptoms, you should see a doctor in time and keep your mind steady. I hope the above can help you