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Cat-eye syndrome (CES) or Schmid–Fraccaro syndrome is a rare condition caused by an abnormal extra chromosome, i.e. a small supernumerary marker chromosome. [2] This chromosome consists of the entire short arm and a small section of the long arm of chromosome 22 .
Cat eye syndrome, caused by the short arm (p) and a small section of the long arm (q) of human chromosome 22 being present three (trisomic) or four times (tetrasomic) instead of the usual two times. The term "cat eye" was coined because of the particular appearance of the vertical colobomas in the eyes of some patients.
It maintains the modern Siamese head and body type but appears in a wide range of coat colors and patterns. Like the Siamese, Orientals have almond-shaped eyes, a triangular head shape, large ears, and an elongated, slender, and muscular body. Their personalities are also very similar. Orientals are social, intelligent, and many are rather vocal.
Cat eyes are similar to brass knuckles but in the shape of a cat face, with sharp and pointy ears that act like small daggers to stab or gouge. People slip their fingers through the spaces of the ...
In humans, the pupil is circular, but its shape varies between species; some cats, reptiles, and foxes have vertical slit pupils, goats and sheep have horizontally oriented pupils, and some catfish have annular types. [3] In optical terms, the anatomical pupil is the eye's aperture and the iris is the aperture stop.
Domestic cat with complete heterochromia, also referred to as an odd-eyed cat. Eye color, specifically the color of the irises, is determined primarily by the concentration and distribution of melanin. Although the processes determining eye color are not fully understood, it is known that inherited eye color is determined by multiple genes ...
The cat was very thin. The grey-furred feline didn’t want to be touched and was in terrible shape. Not only was she clearly dehydrated, she also had two ruptured eyes. ... “Spyro craves human ...
Polycoria is a pathological condition of the eye characterized by more than one pupillary opening in the iris. [1] It may be congenital or result from a disease affecting the iris. [1] It results in decreased function of the iris and pupil, affecting the physical eye and visualization.