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From Wikipedia, the free encyclopedia

Amaurosis (Greek meaning darkening, dark, or obscure) is vision loss or weakness that occurs without an apparent lesion affecting the eye.[1] It may result from either a medical condition or excess acceleration, as in flight. The term is the same as the Latin gutta serena, which means, in Latin, clear drop (or bright drop). Gutta serena is a condition of partial or complete blindness with a transparent, clear pupil. This term contrasts with suffusio nigra which means, in Latin, dark suffusion, indicating partial or complete blindness with a dark pupil, e.g., a cataract. Milton, already totally blind for twelve years (some scholars think from retinal detachment; others have diagnosed glaucoma) by the time he published Paradise Lost, refers to these terms in Book 3, lines 25–26.[2]

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  • Animation: Leber Congenital Amaurosis
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  • What is Amaurosis Fugax? (Temporary Vision Loss)

Transcription

Types

Leber's congenital amaurosis

Leber's congenital amaurosis (LCA) is the most severe and earliest of the inherited retinal dystrophies that cause congenital blindness. It has an incidence of 2-3 per 100,000 births and accounts for 10-18% of cases of congenital blindness among children in blind institutes and 5% of all retinal dystrophies, a figure that is likely to be greater in countries with a greater percentage of consanguinity.[3]

In most cases, LCA is inherited in an autosomal recessive pattern, as established by Alström and Olson in 1957. Some patients only have retinal blindness, whereas others have multi-systemic involvement that includes renal, cardiac, skeletal, and, most notably, central nervous system anomalies.[3]

Theodor von Leber, a German ophthalmologist, described LCA in 1869 as a disorder characterized by profound visual loss present at or shortly after birth, nystagmus, sluggish pupillary reactions, and pigmentary retinopathy.[3]

Amaurosis fugax

Amaurosis fugax, also known as transient monocular blindness, is caused by a sudden, temporary decrease in blood flow to one eye. The loss of vision is abrupt, lasting only seconds or minutes. Blindness is total, though it is sometimes limited to a specific area of vision. Blindness frequently develops as if a shade was drawn upward or downward over the eye, rarely sideward. Single or multiple attacks are possible. Some patients experience hundreds, if not thousands, of episodes. Pain, scintillations, and diplopia are usually not present. The prognosis for retinal recovery is good in most patients; retinal infarction occurs in a few.[4]

Quinidine toxicity

Although amaurosis caused by quinine poisoning is now uncommon, it does occur on occasion. When quinine is used as an abortifacient, the initial history may be deceptive, but the presence of characteristic changes in the fundi usually allows certainty of a diagnosis.[5]

Management

Those experiencing amaurosis are usually advised to consult a physician immediately as any form of vision loss, even if temporary, is a symptom that may indicate the presence of a serious ocular or systemic problem.[citation needed]

In animals

This condition can also occur in ruminants suffering from a vitamin B1 (thiamine) deficiency due to thiamine-related cerebrocortical necrosis (CCN).[citation needed]

References

  1. ^ "Dorlands Medical Dictionary". Archived from the original on 2008-03-03. Retrieved 2005-09-25.
  2. ^ "Amaurosis". The Encyclopedia of World Problems. Retrieved 2023-11-04.
  3. ^ a b c Fazzi, Elisa; Signorini, Sabrina Giovanna; Scelsa, Barbara; Bova, Stefania Maria; Lanzi, Giovanni (2003). "Leber's congenital amaurosis: an update". European Journal of Paediatric Neurology. 7 (1). Elsevier BV: 13–22. doi:10.1016/s1090-3798(02)00135-6. ISSN 1090-3798.
  4. ^ Gautier, Jean-Claude (1993-08-05). "Amaurosis Fugax". New England Journal of Medicine. 329 (6). Massachusetts Medical Society: 426–428. doi:10.1056/nejm199308053290611. ISSN 0028-4793.
  5. ^ Drance, S. M. (1955-03-01). "Quinine Amaurosis". British Journal of Ophthalmology. 39 (3). BMJ: 178–181. doi:10.1136/bjo.39.3.178. ISSN 0007-1161. PMC 1324536.
This page was last edited on 3 January 2024, at 01:08
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