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Type 1 is characterised by congenital sensorineural hearing loss, pigmentary deficiencies of the hair such as a white lock of hair in the front-centre of the head or premature greying, pigmentary deficiencies of the eyes such as different-coloured eyes (complete heterochromia iridum), multiple colours in an eye (sectoral heterochromia iridum) or brilliant blue eyes, patches of skin ...
Central heterochromia is also an eye condition where there are two colors in the same iris; but the arrangement is concentric, rather than sectoral. The central (pupillary) zone of the iris is a different color than the mid-peripheral (ciliary) zone. Central heterochromia is more noticeable in irises containing low amounts of melanin. [32]
For others, colors are triggered when musical notes or keys are being played. People with synesthesia related to music may also have perfect pitch because their ability to see and hear colors aids them in identifying notes or keys. [19] The colors triggered by certain sounds, and any other synesthetic visual experiences, are referred to as ...
This is a list of notable people who have been documented as having heterochromia iridis, a condition when the irises have different colours. People who are frequently mistakenly thought to have heterochromia are not included, but may be listed in the Notes section.
Those that 'see' or perceive the color in external space are called projectors, and those that perceive the color in the mind's eye are often called associators, but these terms can be misleading to understanding the nature of the experience. [2] [3] For most synesthetes, the condition is not wholly sensory/perceptual. [3]
It's designed for people with mild to profound hearing loss and is available in a four-color range of sandalwood/black, copper/black, graphite/black, and silver/black. ... a pediatric app called ...
Usher syndrome, also known as Hallgren syndrome, Usher–Hallgren syndrome, retinitis pigmentosa–dysacusis syndrome or dystrophia retinae dysacusis syndrome, [1] is a rare genetic disorder caused by a mutation in any one of at least 11 genes resulting in a combination of hearing loss and visual impairment.
John Gorman, a former Medicare official and founder of two companies that review records and conduct home visits on behalf of Medicare insurers, doesn’t think the changes will actually fix the ...