Recurrent spontaneous coronary dissections in a patient with a de novo fibrillin-1 mutation without Marfan syndrome

Thromb Haemost. 2015 Mar;113(3):668-70. doi: 10.1160/TH14-11-0913. Epub 2014 Dec 18.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aortic Dissection / complications
  • Aortic Dissection / diagnosis
  • Aortic Dissection / genetics*
  • Aortic Dissection / metabolism
  • Cell Movement
  • Cells, Cultured
  • Coronary Aneurysm / complications
  • Coronary Aneurysm / diagnosis
  • Coronary Aneurysm / genetics*
  • Coronary Aneurysm / metabolism
  • Coronary Angiography
  • DNA Mutational Analysis
  • Fibrillin-1
  • Fibrillins
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Microfilament Proteins / genetics*
  • Microfilament Proteins / metabolism
  • Mutation*
  • Myocardial Infarction / etiology
  • Myocytes, Smooth Muscle / metabolism
  • Myocytes, Smooth Muscle / pathology
  • Phenotype
  • Polymorphism, Single Nucleotide*
  • Recurrence
  • Stem Cells / metabolism
  • Stem Cells / pathology

Substances

  • FBN1 protein, human
  • Fibrillin-1
  • Fibrillins
  • Microfilament Proteins