A rare acquired eye disease with characteristics of progressive visual loss due to bilateral juxta foveolar capillary occlusions, capillary telangiectasia and minimal exudation. It is associated with systemic or cerebral vascular occlusive disease.

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

idiopathische maculaire teleangiëctasie type 3

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Cutis marmorata telangiectasia congenita

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

congenitale livedo reticularis

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Hereditary haemorrhagic telangiectasia

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

hereditaire hemorragische teleangiëctasie

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Anderen hebben gezocht naar : ataxia telangiectasia cutis marmorata telangiectasia congenita hereditary haemorrhagic telangiectasia louis-bar broken veins red spidery marks telangiectasia telangiectasis

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'telangiectasia' ->

Date index: 2024-04-17