Spontaneous coronary dissection in a patient with Beals syndrome

J Cardiovasc Med (Hagerstown). 2021 Dec 1;22(12):e18-e20. doi: 10.2459/JCM.0000000000001200.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Arachnodactyly* / diagnosis
  • Arachnodactyly* / genetics
  • Arachnodactyly* / physiopathology
  • Arachnodactyly* / therapy
  • Contracture* / diagnosis
  • Contracture* / genetics
  • Contracture* / physiopathology
  • Contracture* / therapy
  • Coronary Angiography / methods
  • Coronary Stenosis* / diagnostic imaging
  • Coronary Stenosis* / physiopathology
  • Coronary Stenosis* / surgery
  • Coronary Vessel Anomalies* / diagnostic imaging
  • Coronary Vessel Anomalies* / physiopathology
  • Coronary Vessel Anomalies* / surgery
  • Diagnosis, Differential
  • Drug-Eluting Stents
  • Female
  • Fibrillin-2 / genetics
  • Heart Defects, Congenital / diagnosis
  • Heart Defects, Congenital / etiology
  • Humans
  • Loeys-Dietz Syndrome / diagnosis
  • Loeys-Dietz Syndrome / physiopathology
  • Marfan Syndrome / diagnosis
  • Marfan Syndrome / physiopathology
  • Middle Aged
  • Mutation
  • Percutaneous Coronary Intervention* / instrumentation
  • Percutaneous Coronary Intervention* / methods
  • Treatment Outcome
  • Vascular Diseases / congenital*
  • Vascular Diseases / diagnostic imaging
  • Vascular Diseases / physiopathology
  • Vascular Diseases / surgery

Substances

  • FBN2 protein, human
  • Fibrillin-2

Supplementary concepts

  • Congenital contractural arachnodactyly
  • Coronary Artery Dissection, Spontaneous