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11 relations: Amyloidosis, Ataxia, Cornea, Corneal dystrophy, Corneal transplantation, Cutis laxa, Gelsolin, Ophthalmology, Punctal plug, Recurrent corneal erosion, TGFBI.
Amyloidosis
Amyloidosis is a group of diseases in which abnormal protein, known as amyloid fibrils, builds up in tissue.
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Ataxia
Ataxia is a neurological sign consisting of lack of voluntary coordination of muscle movements that includes gait abnormality.
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Cornea
The cornea is the transparent front part of the eye that covers the iris, pupil, and anterior chamber.
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Corneal dystrophy
Corneal dystrophy is a group of rare hereditary disorders characterised by bilateral abnormal deposition of substances in the transparent front part of the eye called the cornea.
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Corneal transplantation
Corneal transplantation, also known as corneal grafting, is a surgical procedure where a damaged or diseased cornea is replaced by donated corneal tissue (the graft).
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Cutis laxa
Cutis laxa (also known as chalazoderma, dermatochalasia, dermatolysis, dermatomegaly, generalized elastolysis, generalized elastorrhexis, or pachydermatoceleJames, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. Page 515..) is a group of rare connective tissue disorders in which the skin becomes inelastic and hangs loosely in folds.
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Gelsolin
Gelsolin is an actin-binding protein that is a key regulator of actin filament assembly and disassembly.
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Ophthalmology
Ophthalmology is a branch of medicine and surgery (both methods are used) that deals with the anatomy, physiology and diseases of the eyeball and orbit.
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Punctal plug
A punctal plug, also known as tear duct plug or lacrimal plug, is a small medical device that is inserted into the tear duct (puncta) of an eye to block the duct.
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Recurrent corneal erosion
Recurrent corneal erosion is a disorder of the eyes characterized by the failure of the cornea's outermost layer of epithelial cells to attach to the underlying basement membrane (Bowman's layer).
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TGFBI
Transforming growth factor, beta-induced, 68kDa, also known as TGFBI (initially called BIGH3, BIG-H3), is a protein which in humans is encoded by the TGFBI gene, locus 5q31.
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Biber-Haab-Dimmer dystrophy, Finnish amyloidosis, Finnish type amyloidosis, Lattice corneal dystrophy type 2, Lattice corneal dystrophy type I, Lattice corneal dystrophy type II.
