Genetic and Metabolic MedicineTier 1Disease (DEADMAN)

Marfan syndrome

Description

  • AD connective tissue disorder of fibrillin-1 - skeletal, ocular, cardiovascular
  • The aorta is the only part that kills; everything else is a clue to it
Phenotype
  • Skeletal - tall, disproportionately long limbs (arm span : height >1.05), arachnodactyly (wrist + thumb signs), pectus excavatum/carinatum, scoliosis, pes planus, joint hypermobility, high-arched palate with crowded teeth, long narrow face, dolichocephaly, enophthalmos, retrognathia, malar hypoplasia, reduced upper:lower segment ratio (<0.85)
  • Ocular - ectopia lentis (superotemporal displacement, the single most specific feature), myopia, flat cornea, retinal detachment, blue sclerae
  • Cardiovascular - aortic root dilatation at the sinuses of Valsalva -> AR (wide pulse pressure), dissection; MVP with MR; dilated PA; descending aortic aneurysm
  • Other - spontaneous pneumothorax, apical blebs, dural ectasia, recurrent herniae, striae atrophicae

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