Marfan syndrome and Aorta
Marfan Syndrome is an inherited disorder that affects connective tissue. People with Marfan syndrome are tall and thin with long arms, legs, fingers and toes experiencing back pain, mitral valve prolapse or murmur, abnormally raised roof of the mouth or crowded teeth, blurred vision or nearsightedness, bulging chest or sunken chest, along with abnormally long fingers, collapsed lung, disproportionately long arms and legs, double jointed, fatigue, flat feet, scoliosis, small pupils, stretch marks, or tall and slender build. Treatment includes medication to keep blood pressure low, glasses or contact lenses and surgery. The various surgeries such as Vitrectomy, Endovascular aneurysm repair, Vascular grafting and Vascular grafting need to be undergone for its curing.
- Aortic Enlargement
- Aortic Tear or Rupture
- Mitral Valve Prolapse
- Aortic Regurgitation
Related Conference of Marfan syndrome and Aorta
October 22-23, 2025
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November 03-04, 2025
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Marfan syndrome and Aorta Conference Speakers
Recommended Sessions
- Risk Factors of Heart Disease
- Abnormal Heart Rhythms
- Cardiac Anesthesiologist
- Cardiac Diagnosis
- Cardiac Procedures and Surgery
- Cardiology
- Cardiomyopathy
- Cardiovascular and Robotic Surgeries
- Chronic Obstructive Pulmonary Disorder and Forms of reduced lung function
- Coronary Artery Diseases
- Heart Curing Procedures
- High Blood Cholesterol
- Hypertension
- Interventional Cardiology
- Marfan syndrome and Aorta
- Obesity and Diabetes
- Pericardial and Peripheral Vascular diseases
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