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Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin. These basic features constitute type 2 of the condition; in type 1, there is ...
Grey eyes make up about 3 percent of the world's population—the second rarest eye color. There are also rare cases of violet and red-colored eyes.
The irises of human eyes exhibit a wide spectrum of colours. Eye color is a polygenic phenotypic trait determined by two factors: the pigmentation of the eye 's iris [ 1 ][ 2 ] and the frequency-dependence of the scattering of light by the turbid medium in the stroma of the iris. [ 3 ]: 9. In humans, the pigmentation of the iris varies from ...
Heterochromia iridum. Heterochromia is a variation in coloration most often used to describe color differences of the iris, but can also be applied to color variation of hair [1] or skin. Heterochromia is determined by the production, delivery, and concentration of melanin (a pigment). It may be inherited, or caused by genetic mosaicism ...
According to the World Atlas, only about five percent of the world's population have hazel eyes—just behind the rarest eye color, which is green. The rarity of hazel eyes can be attributed to ...
Light brown iris with a distinct limbal ring. A limbal ring is a dark ring around the iris of the eye, where the sclera meets the cornea. [1] It is a dark-colored manifestation of the corneal limbus resulting from optical properties of the region. [2] The appearance and visibility of the limbal ring can be negatively affected by a variety of ...
Monochromacy (from Greek mono, meaning "one" and chromo, meaning "color") is the ability of organisms to perceive only light intensity without respect to spectral composition. Organisms with monochromacy lack color vision and can only see in shades of grey ranging from black to white. Organisms with monochromacy are called monochromats.
Specialty. Ophthalmology, dermatology. Oculocutaneous albinism is a form of albinism involving the eyes (oculo-), the skin (- cutaneous), and the hair. [1] Overall, an estimated 1 in 20,000 people worldwide are born with oculocutaneous albinism. [1] OCA is caused by mutations in several genes that control the synthesis of melanin within the ...