
KEGH - Wikipedia
KEGH (107.1 FM) is an American radio station broadcasting a Spanish adult contemporary format. It is licensed to Woodruff, Utah, United States, and owned by Michael V. Call, through licensee Aerostar Communications, LLC. [2] . In February 2009, KEGH was a simulcast of KEGA, The Eagle 101.5, according to the Simmons Media corporate web site. [3]
Keratoendotheliitis Fugax Hereditaria - EyeWiki
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.
KEFH - Wikipedia
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 | Hereditary Ocular Diseases
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.
Keratoendotheliitis Fugax Hereditaria - MalaCards
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.
Keratitis fugax hereditaria - NIH Genetic Testing Registry (GTR)
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.
Entry - #148200 - KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH …
2018年3月8日 · 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.
Keratitis fugax hereditaria (Concept Id: C1835697)
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.
KEFH | Hereditary Ocular Diseases
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.
KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH - OMIM
Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text, referenced overviews in OMIM contain information on …