KEFH (99.3 FM) is a radio station broadcasting a classic hits format. Licensed to Clarendon, Texas, United States, it serves the Amarillo area. The station is currently owned by Donna and …

Keratoendotheliitis fugax hereditaria is an autosomal dominant condition that results in episodic debilitating inflammatory attacks that result in unilateral pain, corneal edema and opacification, conjunctival injection, and a decrease in visual acuity; these episodes last 2-5 days.

Mar 1, 2024 · Keratoendotheliitis fugax hereditaria is a rare inflammatory genetic condition characterized by recurrent episodes of debilitating unilateral corneal and conjunctival hyperemia, corneal edema, visual impairment, corneal opacification, and photophobia that last for 2 to 5 days.

Keratoendotheliitis fugax hereditaria is an autosomal dominantly inherited disease of the cornea, caused by a point mutation in cryopyrin [1] (also known as NALP3) that in humans is encoded by the NLRP3 gene [2] located on the long arm of chromosome 1. [3]

Recurrent ocular inflammatory episodes begin between the ages of 3 and 12 years (median age of onset 11 years). These episodes can last from a few days to several weeks and may recur several times a year. Episodes are milder and less frequent in older individuals.

Mar 8, 2018 · Keratoendotheliitis fugax hereditaria (KEFH) is an autosomal dominant corneal disease that periodically and fleetingly affects the corneal endothelium, stroma, and vision, eventually resulting in central corneal stromal opacities in some patients.

Keratoendotheliitis fugax hereditaria (KEFH) is an autosomal dominant corneal disease that periodically and fleetingly affects the corneal endothelium, stroma, and vision, eventually resulting in central corneal stromal opacities in some patients.

Keratoendotheliitis fugax hereditaria (KEFH) is an autosomal dominant corneal disease that periodically and fleetingly affects the corneal endothelium, stroma, and vision, eventually resulting in central corneal stromal opacities in some patients.

Keratoendotheliitis Fugax Hereditaria (KEFH) is a rare genetic disorder that affects the corneal endothelium and leads to recurrent episodes of corneal edema. Learn about the causes, symptoms, and treatment options for KEFH.

Keratoendotheliitis fugax hereditaria is an autoinflammatory cryopyrin-associated periodic syndrome caused by a missense mutation c.61G>C in exon 1 of NLRP3 in Finnish patients. It is additionally expected to occur in other populations of European descent.