Illustration of the eye retina in Tay-Sachs disease (abbreviated TSD, also known as GM2 gangliosidosis, Hexosaminidase A deficiency or Sphingolipidosis), a genetic disorder, fatal in its most common variant known as Infantile Tay-Sachs disease. All patients with Tay-Sachs disease have a ''cherry-red'' spot, easily observable by a physician using an ophthalmoscope, in the back of their eyes.
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Details
Creative#:
TPG33142583
Source:
達志影像
Authorization Type:
RF
Release Information:
須由TPG 完整授權
Model Release:
N/A
Property Release:
N/A
Right to Privacy:
No
Same folder images:
autosomalrecessivedisordercherryredspotdiseasedisordereyegeneticdisordergm2gm2gangliosidosishexosaminidaseadeficiencylipidstoragedisorderlysosomalstoragediseasemaculamedicalmetabolicdisorderneurologyocularophthalmologyophthalmologypathologyrarediseaseredspotretinasphingolipidosistay-sachsdiseasetsdartworkillustration
aartworkautosomalcherrydeficiencydiseasediseasediseasediseasedisorderdisorderdisorderdisorderdisordereyegangliosidosisgeneticgm2gm2hexosaminidaseillustrationlipidlysosomalmaculamedicalmetabolicneurologyocularophthalmologyophthalmologypathologyrarerecessiveredredretinasphingolipidosisspotspotstoragestoragetay-sachstsd