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. | |
Licence : | Libre de droits |
Crédit: | Science Photo Library / Kon, Kateryna |
Model Release : | Non requis |
Property Release : | Non requis |
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