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What (who) is quinine amaurosis - definition
RETINAL DISEASE THAT IS CHARACTERIZED BY NYSTAGMUS, SLUGGISH OR NO PUPILLARY RESPONSES, AND SEVERE VISION LOSS OR BLINDNESS
Leber's congenital amaurosis; Leber Congenital Amaurosis; Leber's Congenital Amaurosis; Amaurosis congenita of Leber; Leber amaurosis; Amaurosis congenita of Leber, type 1; Amaurosis congenita of Leber, type 2; Congenital amaurosis; Leber's amaurosis
quinine
![fluoresce]] under black light.](https://commons.wikimedia.org/wiki/Special:FilePath/Tonic water uv.jpg?width=200 "fluoresce]] under black light.")
CHEMICAL COMPOUND
Quinine powder; Quinnine; Bromo Quinine; Bromo quinine; ATC code P01BC01; Qualaquin; Aflukin; Chinin; Chinine; Coco-Quinine; Kinine; Legatrin; Quinologist; Quinine Sulfate; Quinine bisulfate heptahydrate; Quinine bisulfate; Quinbisul
Quinine is a drug that is used to treat fevers such as malaria.
N-UNCOUNT
Quinine
CHEMICAL COMPOUND
Quinine powder; Quinnine; Bromo Quinine; Bromo quinine; ATC code P01BC01; Qualaquin; Aflukin; Chinin; Chinine; Coco-Quinine; Kinine; Legatrin; Quinologist; Quinine Sulfate; Quinine bisulfate heptahydrate; Quinine bisulfate; Quinbisul
·noun An alkaloid extracted from the bark of several species of cinchona (·esp. Cinchona Calisaya) as a bitter white crystalline substance, C20H24N2O2. Hence, by extension (Med.), any of the salts of this alkaloid, as the acetate, chloride, sulphate, ·etc., employed as a febrifuge or antiperiodic. Called also quinia, quinina, ·etc.
quinine
CHEMICAL COMPOUND
Quinine powder; Quinnine; Bromo Quinine; Bromo quinine; ATC code P01BC01; Qualaquin; Aflukin; Chinin; Chinine; Coco-Quinine; Kinine; Legatrin; Quinologist; Quinine Sulfate; Quinine bisulfate heptahydrate; Quinine bisulfate; Quinbisul
['kw?ni:n, kw?'ni:n]
¦ noun a bitter crystalline compound present in cinchona bark, used as a tonic and formerly as an antimalarial drug.
Origin
C19: from Sp. quina 'cinchona bark' (from Quechua kina 'bark') + -ine4.
Wikipedia
Leber congenital amaurosis
Leber congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life.
It affects about 1 in 40,000 newborns. LCA was first described by Theodor Leber in the 19th century. It should not be confused with Leber's hereditary optic neuropathy, which is a different disease also described by Theodor Leber.
One form of LCA was successfully treated with gene therapy in 2008.
