Hereditary hemorrhagic telangiectasia and factor viii inhibitor

Alex Sudarshan, Ethan Natelson, Craig Gordon

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


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
Issue number5
StatePublished - Jan 1 1985

ASJC Scopus subject areas

  • Medicine(all)


Dive into the research topics of 'Hereditary hemorrhagic telangiectasia and factor viii inhibitor'. Together they form a unique fingerprint.

Cite this