Keratoendotheliitis fugax hereditaria
id:
keratoendotheliitis-fugax-hereditaria-295-9286607
title:
Keratoendotheliitis fugax hereditaria
text:
Keratoendotheliitis fugax hereditaria is an autosomal dominantly inherited disease of the cornea, caused by a point mutation in cryopyrin that in humans is encoded by the NLRP3 gene located on the long arm of chromosome 1. In keratoendotheliitis fugax hereditaria, patients suffer from periodical transient inflammation of the corneal endothelium and stroma, leading to short term obscuration of vision and, in some patients after repeated attacks, to central corneal stromal opacities. Approximately
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Keratoendotheliitis_fugax_hereditaria
date created:
date modified:
2024-01-09T13:01:52Z
main entity:
{"identifier":"Q55615849","url":"https://www.wikidata.org/entity/Q55615849"}
image:
fields total:
13
integrity:
14