Cancer

  | Above diagram from Endokeratoplasty for Decompensated corneal Endothelium Used by license of the Australian Government | Acknowledgements: The National Organization for Rare roughnesss (NORD) | pain Subdivisions epithelial basement membrane dystrophy granular corneal dystrophy type I lattice corneal dystrophy type I & type 2 macular corneal dystrophy Meesmann corneal dystrophy General Discussion corneal dystrophies are a group of genetic, often progressive, centre disorders in which abnormal material often accumulates in the clear (transparent) bring out layer of the pith (cornea). Corneal dystrophies may not trend symptoms (asymptomatic) in some individuals; in others they may cause of entailment vision impairment. The age of onset and special symptoms vary among the confused forms of corneal dystrophy. The disorders have some similar characteristics; most forms of corneal dystrophy affect both eyes (bilateral), progress slowly, do not affect other areas of the body, and tend to run in families. Most forms are inherited as autosomal paramount traits; a few are inherited as autosomal recessive traits.

An international classification of the corneal dystrophies has been developed that takes into story the chromosomal loci of the various corneal dystrophies as well as the responsible genes and their mutations. Traditionally, these disorders have classified based upon their clinical findings and the small layer of the cornea affected. Advances in molecular genetics (e.g., identification of peculiar(preno minal) disease genes) have led to a greater ! reason of these disorders. Symptoms The symptoms of corneal dystrophies result from the accumulation of abnormal material at heart the cornea, the clear outer layer of the eye. The cornea serves two functions; it protects the breathe of the eye from dust, germs and other harmful or irritating material, and it acts as the eyes outermost lens, The cornea must remain clear...If you hope to gear up a full essay, order it on our website: OrderCustomPaper.com

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