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| navigate by keyword : taysachs disease tsd retina autosomal recessive disorder cherry red spot eye genetic gm2 gangliosidosis hexosaminidase deficiency lipid storage lysosomal macula metabolic neurology ocular ophthalmology pathology science sphingolipidosis illustration ophthalmoscope hexa betahexosaminidase human enzyme congenital demyelination diagram gene mutation ganglioside inherited lysosome ashkenazi jew niemannpick dysfunction sphingolipid metabolism neurodegeneration sandhoff | ||||||||||||||||||||||||||||||||||||||||
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| Eye retina in sphingolipid storage diseases, 3D illustration. Macular cherry red spot. Tay-Sachs disease and Niemann Pick disease | ||||||||||||||||||||||||||||||||||||||||
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