Literature DB >> 546006

Ocular lesions in hereditary haemorrhagic telangiectasia.

I Vase, P Vase.   

Abstract

A regional survey has been carried out in order to establish the prevalence of hereditary haemorrhagic telangiectasia (HHT) (Rendu-Osler-Weber's disease). Forty-seven patients fulfilled the proband criteria. No patient was registered due to ocular symptoms. All of the probands were subjected to ophthalmological examination in order to estimate the distribution of ocular lesions in HHT. Conjunctival lesions were found in 20 cases, and an intraocular vascular abnormality in only one case. The possibility of intraocular lesions being a component of the clincal picture of HHT or a sporadic vascular abnormality is discussed.

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Mesh:

Year:  1979        PMID: 546006     DOI: 10.1111/j.1755-3768.1979.tb00541.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN: 0001-639X


  10 in total

Review 1.  Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.

Authors:  C L Shovlin; M Letarte
Journal:  Thorax       Date:  1999-08       Impact factor: 9.139

2.  Identification of Retinal Vascular Lesions Using Ultra-Widefield Angiography in Hereditary Hemorrhagic Telangiectasia Patients.

Authors:  Sampat Sindhar; Bliss E O'Bryhim; Jordan Licata; Jay F Piccirillo; Rajendra S Apte
Journal:  Ophthalmol Retina       Date:  2019-02-15

3.  Hereditary hemorrhagic telangiectasia with multiple fusiform retinal aneurysms.

Authors:  Nagihan Uğurlu; Selma Emre; Fatma Yülek; Emine Kalkan Akcay; Ahmet Sengun
Journal:  J Ocul Biol Dis Infor       Date:  2013-01-29

4.  Spontaneous thrombosis of an orbital arteriovenous malformation revealing hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease). A case report.

Authors:  Charles Van Went; A Ozanne; G Saliou; G Dethorey; I De Monchy; T Krings; D Ducreux; M Labetoulle
Journal:  Interv Neuroradiol       Date:  2011-12-16       Impact factor: 1.610

5.  The value of screening for multiple arterio-venous malformations in hereditary hemorrhagic telangiectasia: a diagnostic study.

Authors:  Benedikt J Folz; Ana Cerra Wollstein; Heiko Alfke; Anja A Dünne; Burkard M Lippert; Konrad Görg; Hans-Joachim Wagner; Siegfried Bien; Jochen A Werner
Journal:  Eur Arch Otorhinolaryngol       Date:  2003-12-17       Impact factor: 2.503

6.  Prevalence of ocular manifestations in hereditary hemorrhagic telangiectasia.

Authors:  Urban W Geisthoff; Konrad Hille; Klaus W Ruprecht; Thomas Verse; Peter K Plinkert
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2007-08       Impact factor: 3.535

7.  Severe open angle glaucoma in hereditary hemorrhagic telangiectasia.

Authors:  Rachel W Kuchtey; George T Naratadam; John Kuchtey
Journal:  Clin Case Rep       Date:  2015-06-18

8.  Ocular lesions in hereditary hemorrhagic telangiectasia: genetics and clinical characteristics.

Authors:  Inés Gómez-Acebo; Sara Rodríguez Prado; Ángel De La Mora; Roberto Zarrabeitia Puente; Beatriz de la Roza Varela; Trinidad Dierssen-Sotos; Javier Llorca
Journal:  Orphanet J Rare Dis       Date:  2020-06-29       Impact factor: 4.123

Review 9.  An update on the ophthalmic features in hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

Authors:  Solmaz Abdolrahimzadeh; Martina Formisano; Carla Marani; Siavash Rahimi
Journal:  Int Ophthalmol       Date:  2022-01-16       Impact factor: 2.029

10.  Endothelial depletion of Acvrl1 in mice leads to arteriovenous malformations associated with reduced endoglin expression.

Authors:  Simon Tual-Chalot; Marwa Mahmoud; Kathleen R Allinson; Rachael E Redgrave; Zhenhua Zhai; S Paul Oh; Marcus Fruttiger; Helen M Arthur
Journal:  PLoS One       Date:  2014-06-04       Impact factor: 3.240

  10 in total

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