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Fuchs dystrophy, also referred to as Fuchs endothelial corneal dystrophy ( FECD) and Fuchs endothelial dystrophy ( FED ), is a slowly progressing corneal dystrophy that usually affects both eyes and is slightly more common in women than in men. Although early signs of Fuchs dystrophy are sometimes seen in people in their 30s and 40s, the disease rarely affects vision until people reach their ...
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.
Epithelial basement membrane dystrophy ( EBMD) is a disorder of the eye that can cause pain and dryness. It is sometimes included in the group of corneal dystrophies. [1] It diverges from the formal definition of corneal dystrophy since it is non-familial in most cases. It also has a fluctuating course, while for a typical corneal dystrophy the ...
Leber's hereditary optic neuropathy ( LHON) is a mitochondrially inherited (transmitted from mother to offspring) degeneration of retinal ganglion cells (RGCs) and their axons that leads to an acute or subacute loss of central vision; it predominantly affects young adult males. LHON is transmitted only through the mother, as it is primarily due ...
Retinitis pigmentosa ( RP) is a genetic disorder of the eyes that causes loss of vision. [1] Symptoms include trouble seeing at night and decreasing peripheral vision (side and upper or lower visual field). [1] As peripheral vision worsens, people may experience " tunnel vision ". [1] Complete blindness is uncommon. [2] Onset of symptoms is generally gradual and often begins in childhood. [1] [2]
Overview The importance of Fuchs' life achievement must surely be based on his discovery and description of numerous ocular diseases and abnormalities. As a result of more than 250 scientific publications, the name Ernst Fuchs became well known throughout the world. Although his name is commonly recognized in conjunction with various corneal and anterior segment disorders, Ernst Fuchs ...
Damage caused by the hereditary condition known as Fuchs dystrophy (q.v.)—where Descemet's membrane progressively fails and the cornea thickens and clouds because the exchange of nutrients/fluids between the cornea and the rest of the eye is interrupted—can be reversed by surgery.
Muscle–eye–brain ( MEB) disease, also known as muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A3 ( MDDGA3 ), [2] is a kind of rare congenital muscular dystrophy (CMD), largely characterized by hypotonia at birth. Patients have muscular dystrophy, central nervous system abnormalities and ocular abnormalities. The condition is degenerative.