Amaurosis fugax differential diagnosis: Difference between revisions
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==Overview== | |||
[[Leber's congenital amaurosis]] is an inherited disease resulting in severe vision loss or blindness that was first described by Theodore Leber in the 19th century. Amaurosis can also occur in ruminants suffering from a [[vitamin B1]] ([[Thiamin]]) deficiency due to Thiamine-Related Cerebrocortical Necrosis (CCN). | |||
==References== | ==References== | ||
{{reflist|2}} | |||
[[Category:Needs content]] | [[Category:Needs content]] | ||
[[Category:Cardiovascular diseases]] | [[Category:Cardiovascular diseases]] | ||
[[Category:Ophthalmology]] | [[Category:Ophthalmology]] | ||
[[Category:Neurology]] | [[Category:Neurology]] | ||
[[Category:Ddx]] | [[Category:Ddx]] | ||
Latest revision as of 19:24, 29 May 2015
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Amaurosis fugax Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Amaurosis fugax differential diagnosis On the Web |
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American Roentgen Ray Society Images of Amaurosis fugax differential diagnosis |
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Risk calculators and risk factors for Amaurosis fugax differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Overview
Leber's congenital amaurosis is an inherited disease resulting in severe vision loss or blindness that was first described by Theodore Leber in the 19th century. Amaurosis can also occur in ruminants suffering from a vitamin B1 (Thiamin) deficiency due to Thiamine-Related Cerebrocortical Necrosis (CCN).