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OR2‐011 : Case report: severe bleeding phenotype due to undiagnosed α2 antiplasmin deficiency with novel gene mutation identified

Researchers

Presenter

  • A Zaidi

Principal Investigators

  • S Sivapalaratnam

  • S Platton

  • L Bowles

  • J Pasi

  • D Hart

Medical Centers

  • Paediatrics, Royal London Hospital Barts Health NHS Trust, London,United Kingdom

Locations

  • United Kingdom

Companies

  • N/A

Study Components

Therapeutic Area

  • Blood/haematological Diseases

Disease

  • N/A

Biomarkers

  • Activated partial thromboplastin time

Drug/Treatment

  • Tranexamic acid

  • Caprilon

  • Fibrinogen (IV)

  • Evithrom

Outcome

  • N/A

Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A

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