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

February 04-05, 2021

5th Annual Summit on Rare Diseases and Orphan Drugs

Bangkok, Thailand
February 25-26, 2021

4th World Congress on Pathology and Clinical Practice

Vienna, Austria
March 24-25, 2021

3rd Pathology and Infectious Disease Conference

Paris, France
April 08-09, 2021

17th Global Experts Meeting on Pathology and Laboratory Medicine

Port Moresby, New Guinea
April 12-13, 2021

18th Asia Pacific Pathology Congress

Tokyo, Japan
October 19-20, 2021

Global pathologists meet

Manila, Philippines
October 19-20, 2021

World Congress on Pathology and Microbiology

Angeles, Philippines

Marfan syndrome and Aorta Conference Speakers

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