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Phantom sensations in Phantom Eye Syndrome (PES) encompass various tactile perceptions such as paresthesia, dysesthesia, and hyperpathia, excluding pain. These sensations can manifest in different forms, including kinetic, kinesthetic, or exteroceptive perceptions, and are commonly experienced by almost all PES patients. [ 4 ]
Phantom eye syndrome can occur after eye loss. The pain sensation and its duration and frequency varies from individual to individual. Phantom pain should be distinguished from other conditions that may present similarly, such as phantom limb sensation and residual limb pain.
The syndrome is discussed in: Vilayanur S. Ramachandran's book Phantoms in the Brain. Ramachandran suggests that James Thurber, who was blinded in one eye as a child, may have derived his extraordinary imagination from the syndrome. [25] Vikram Chandra's book Sacred Games (2006) David Eagleman's book Incognito: The Secret Lives of the Brain
Peutz–Jeghers syndrome; Pfeiffer syndrome; Phantom eye syndrome; Phantom limb; Phantom vibration syndrome; Phelan-McDermid Syndrome; Pickwickian syndrome; Pigment dispersion syndrome; Pigmented hairy epidermal nevus syndrome; Pilotto syndrome; Piriformis syndrome; Pitt–Hopkins syndrome; Plica syndrome; Plummer–Vinson syndrome; POEMS ...
29-year-old Caitin Stickels, from Seattle, was born with Schmid-Fraccaro, also known as "Cat Eye Syndrome". The genetic disorder is known to cause an array of issues, the most visible of which ...
Every normal mammalian eye has a scotoma in its field of vision, usually termed its blind spot. This is a location with no photoreceptor cells, where the retinal ganglion cell axons that compose the optic nerve exit the retina. This location is called the optic disc. There is no direct conscious awareness of visual scotomas.
Graziadei said that the whites of his eyes can sometimes look jaundiced, or more yellow, as a result of the condition. He said it tends to impact him more when he is worn out. "I am healthy.
Ataxia telangiectasia (Louis–Bar syndrome) Encephalotrigeminal angiomatosis (Sturge–Weber syndrome) (encephalofacial cavernous hemangiomatosis) Neurofibromatosis (von Recklinghausen's disease) Tuberous sclerosis (Bourneville's syndrome) Wyburn–Mason syndrome (racemose hemangiomatosis)
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