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  2. Cherry-red spot - Wikipedia

    en.wikipedia.org/wiki/Cherry-red_spot

    The sign was first described by Warren Tay, founding member of the British Ophthalmological Society, in 1881, with reference to a patient with TaySachs disease. The cherry red spot is seen in central retinal artery occlusion, appearing several hours after the blockage of the retinal artery occurs. [ 4 ]

  3. Tay–Sachs disease - Wikipedia

    en.wikipedia.org/wiki/TaySachs_disease

    TaySachs disease; Other names: GM2 gangliosidosis, hexosaminidase A deficiency [1] Cherry-red spot as seen in the retina in TaySachs disease. The fovea's center appears bright red because it is surrounded by a whiter than usual area. Specialty: Medical genetics: Symptoms: Initially: Decreased ability to turn over, sit, or crawl [1]

  4. GM2-gangliosidosis, AB variant - Wikipedia

    en.wikipedia.org/wiki/GM2-gangliosidosis,_AB_variant

    This cherry-red spot is the same finding that Warren Tay first reported in 1881, when he identified a case of TaySachs disease, and it has the same etiology. [5] The prognosis for AB variant is the same as for infantile TaySachs disease. Children with AB variant die in infancy or early childhood. [citation needed]

  5. Central retinal artery occlusion - Wikipedia

    en.wikipedia.org/wiki/Central_retinal_artery...

    Cherry red spot in a person with central retinal artery occlusion. Central retinal artery occlusion is characterized by painless, acute vision loss in one eye. [1] Upon fundoscopic exam, one would expect to find: cherry-red spot (90%) (a morphologic description in which the normally red background of the choroid is sharply outlined by the swollen opaque retina in the central retina), retinal ...

  6. Waren Tay - Wikipedia

    en.wikipedia.org/wiki/Waren_Tay

    In 1881, Waren (often misspelt Warren) Tay first described the red spot on the retina of the eye that is present in TaySachs disease. [1] He reported this condition in the Volume I edition of the Ophthalmological Society, an organization in which he was a founding member. Here he described the symptoms in a child who also had neurological ...

  7. GM2 gangliosidoses - Wikipedia

    en.wikipedia.org/wiki/GM2_gangliosidoses

    TaySachs disease is a rare autosomal recessive genetic disorder that causes a progressive deterioration of nerve cells and of mental and physical abilities that begins around six months of age and usually results in death by the age of four. It is the most common of the GM2 gangliosidoses.

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  9. Central retinal artery - Wikipedia

    en.wikipedia.org/wiki/Central_retinal_artery

    The entire retina (with the exception of the fovea) becomes pale and swollen and opaque while the central fovea still appears reddish (this is because the choroid color shows through). This is the basis of the famous "Cherry red spot" seen on examination of the retina on funduscopy of a central retinal artery occlusion (CRAO).

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