HEREDITARY HEMORRHAGIC TELANGIECTASIA

Messody Zagury; Marcos B.V. Albers; Sergio Felberg; Adriana V Portes; M. Cristina Nishiwaki-Dantas; Paulo E.C. Dantas

doi:10.15324/vpa.v14i1.243

Vision Pan-America (Mar 2015)

HEREDITARY HEMORRHAGIC TELANGIECTASIA

Messody Zagury,
Marcos B.V. Albers,
Sergio Felberg,
Adriana V Portes,
M. Cristina Nishiwaki-Dantas,
Paulo E.C. Dantas

Affiliations

Messody Zagury: Corneal and External Disease Service, Department of Ophthalmology, Santa Casa of São Paulo, Brasil
Marcos B.V. Albers: Corneal and External Disease Service, Department of Ophthalmology, Santa Casa of São Paulo, Brasil
Sergio Felberg: Corneal and External Disease Service, Department of Ophthalmology, Santa Casa of São Paulo, Brasil
Adriana V Portes: Corneal and External Disease Service, Department of Ophthalmology, Santa Casa of São Paulo, Brasil
M. Cristina Nishiwaki-Dantas: Corneal and External Disease Service, Department of Ophthalmology, Santa Casa of São Paulo, Brasil
Paulo E.C. Dantas: Professor of Ophthalmology, Corneal and External Disease Service, Department of Ophthalmology, Santa Casa of São Paulo, Brasil

DOI: https://doi.org/10.15324/vpa.v14i1.243
Journal volume & issue: Vol. 14, no. 1
pp. 20 – 21

Abstract

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We describe a patient with clinical history of intermittent haemolacria associated to hereditary hemorrhagic telangiectasia, first seen and diagnosed by the ophthalmologist.

Osler-Weber-Rendu disease, hereditary hemorrhagic telangiectasia, conjunctival telangiectasia.

Published in Vision Pan-America

ISSN: 2219-4665 (Print); 2219-4673 (Online)
Publisher: Pan-American Association of Ophthalmology
Country of publisher: United States
LCC subjects: Medicine: Ophthalmology
Website: https://journals.lww.com/pajo/Pages/default.aspx

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