Hereditary hemorrhagic telangiectasia and factor viii inhibitor

Alex Sudarshan, Ethan Natelson, Craig Gordon

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

A patient with hereditary hemorrhagic telangiectasia manifested recurrent gastrointestinal bleeding aggravated by an acquired factor VIII inhibitor. Immunosuppressive therapy with cyclophosphamide and prednisone successfully corrected the coagulation defect.

Original languageEnglish (US)
Pages (from-to)623-624
Number of pages2
JournalSouthern Medical Journal
Volume78
Issue number5
DOIs
StatePublished - Jan 1 1985

ASJC Scopus subject areas

  • Medicine(all)

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