Eye retina in Tay-Sachs Disease, illustration - stock photo

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.
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.
Eye retina in Tay-Sachs Disease, illustration
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KATERYNA KON/SCIENCE PHOTO LIBRARY
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