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![Tay–Sachs disease - Wikipedia, the free encyclopedia]()
en.wikipedia.orgTay–Sachs disease (also known as GM2 gangliosidosis or hexosaminidase A deficiency ) is a rare autosomal recessive genetic disorder. In its most common variant (known as infantile Tay–Sachs disease), it causes a progressive deterioration of nerve cells an瀏覽：861 -
![Ophthalmological manifestations of Fabry disease - National Center ...]()
www.ncbi.nlm.nih.govOphthalmological manifestations are common in Fabry disease and result from the progressive ... Cornea verticillata was the most frequently reported ophthalmic abnormality in both hemizygous males ...瀏覽：860
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日期：2024-05-13
Optom Vis Sci. 2013 Feb;90(2):e63-78. doi: 10.1097/OPX.0b013e31827ec7eb.
Fabry disease: a review of ophthalmic ......
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日期：2024-05-09
Br J Ophthalmol. 2007 Feb;91(2):210-4. Epub 2006 Sep 14. Ocular
manifestations of Fabry's disease: data from the ......
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日期：2024-05-16
Research from JAMA Ophthalmology — The Ocular Manifestations in Fabry's
Disease....
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日期：2024-05-15
Patients with Fabry disease often present with corneal opacities. ... Downloads.
Ophthalmologists' Disease Sheet (PDF)....
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日期：2024-05-16
Ocular Features of Fabry Disease: Diagnosis of a Treatable Life-threatening
Disorder. Nasi Samiy. x. Nasi Samiy....
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日期：2024-05-15
Department of Ophthalmology and Center for Medical Genetics, Ghent University
Hospital. Ocular Features of ... are currently treatable with ERT: Fabry disease,
mucopolysaccharidosis. (MPS) types I, II, ......
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日期：2024-05-16
Early Detection of Fabry Disease – The Important Role of Ophthalmology. Colin
Willoughby. European Ophthalmic ......
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日期：2024-05-10
21 Feb 2005 ... Amiodarone; Chloroquine and Hydroxychloroquine; Indomethacin;
Phenothiazines; Fabry disease ......
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