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== | ||
Revision as of 15:15, 26 November 2012
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Amaurosis fugax Microchapters |
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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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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).