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Glaucoma is a group of eye diseases that lead to damage of the optic nerve, which transmits visual information from the eye to the brain. Glaucoma may cause vision loss if left untreated. It has been called the "silent thief of sight" because the loss of vision usually occurs slowly over a long period of time. [ 5]
Kearns–Sayre syndrome ( KSS), oculocraniosomatic disorder or oculocranionsomatic neuromuscular disorder with ragged red fibers is a mitochondrial myopathy with a typical onset before 20 years of age. KSS is a more severe syndromic variant of chronic progressive external ophthalmoplegia (abbreviated CPEO), a syndrome that is characterized by ...
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.
1:30,000 to 1:50,000. 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 ...
Phacomorphic glaucoma is an eye disease that can occur due to a neglected advanced cataract.In this, the mature cataractous lens cause secondary angle closure glaucoma.The presence of an asymmetric mature cataractous lens, shallow or closed anterior chamber angle, raised intraocular pressure (IOP) and other typical signs and symptoms of angle-closure glaucoma in the eye may lead to a diagnosis ...
Glaucoma is an eye disease often characterized by increased pressure within the eye or intraocular pressure (IOP). [60] Glaucoma causes visual field loss as well as severs the optic nerve. [61] Early diagnosis and treatment of glaucoma in patients is imperative because glaucoma is triggered by non-specific levels of IOP. [61]
H15-H22 Disorders of sclera, cornea, iris and ciliary body. (H15.0) Scleritis — a painful inflammation of the sclera. (H16) Keratitis — inflammation of the cornea. (H16.0) Corneal ulcer / Corneal abrasion — loss of the surface epithelial layer of the eye's cornea. (H16.1) Snow blindness / Arc eye — a painful condition caused by exposure ...
Genetic. Diagnostic method. Slit lamp. Treatment. None. Stargardt disease is the most common inherited single-gene retinal disease. [ 1] In terms of the first description of the disease, [ 2] it follows an autosomal recessive inheritance pattern, which has been later linked to bi-allelic ABCA4 gene variants (STGD1).
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