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Updated: Dec 26 2021

Marfan Syndrome

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  • Snapshot
    • A 32-year-old man presents to the emergency room for sudden onset of severe chest pain that radiates down his back. Physical exam reveals a tall and thin habitus, arachnodactyly, and pectus excavatum. Radiography shows widened mediastinum, concerning for an aortic dissection.
  • Introduction
    • Clinical definition
      • inherited connective tissue disorder characterized by aortic abnormalities and musculoskeletal deformities
  • Epidemiology
    • Demographics
      • clinical manifestations typically occur in adulthood
  • Etiology
    • Pathogenesis
      • fibrillins form a major part of connective tissues and provide structural support and elasticity to blood vessels, skin, and bones
      • abnormalities in fibrillin can result in
        • aortic abnormalities (cystic medial necrosis)
        • ectopic lens (structural weakness in ligaments of the lens)
        • skeletal deformities
    • Genetics
      • inheritance pattern
        • autosomal dominant
      • mutations
        • FBN1 gene is on chromosome 15 and encodes fibrillin-1, a glycoprotein that forms a protective sheath around elastin
  • Imaging
    • Transthoracic echocardiography
      • indication
        • for all patients to evaluate for cardiac involvement
      • findings
        • mitral or aortic valve abnormalities
        • aortic aneurysm or dissection
  • Studies
    • Making the diagnosis
      • based on clinical presentation
      • genetic testing is not always necessary but is diagnostic
  • Differential
    • Homocystinuria
      • distinguishing factor
        • lens subluxation is downwards
        • mental retardation
    • Ehlers-Danlos syndrome
      • distinguishing factor
        • hyperextensible skin and easy bruising
        • middle-sized artery aneurysms > aortic aneurysms
  • Complications
    • Aortic dissection
      • most common cause of death
    • Mitral valve prolapse
    • Congestive heart failure from cardiac valve abnormalities
  • Prognosis
    • Survival has improved with better management of aortic disease
    • With early diagnosis and management, patients often have a normal life expectancy
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Question
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Orthopedics | Marfan Syndrome
  • Orthopedics
  • - Marfan Syndrome
13:19 min
6/30/2022
60 plays
5.0
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Private Note