Age-related macular degeneration (AMD) is one of the most common causes of vision loss among adults over age 55 living in developed countries. It is caused by the breakdown of the macula, the central part of the retina located in the back of the eye. The macula allows people to see objects directly in front of them (called central vision), as well as fine visual details. People with AMD usually have blurred central vision, difficulty seeing details and colors, and they may notice distortion of straight lines.
The normal function of the macula and AMD is best understood accompanying a description of normal eye function. The eye is made up of many layers of different types of cells that all work together to send images from the environment to the brain, similar to the way a camera records images. When light enters the eye, it passes through the lens and lands on the retina, a very thin tissue, which lines the inside of the eye. The retina is made up of 10 different layers of specialized cells, which allow it to function similarly to film in a camera, by recording images. The macula is a small, yellow-pigmented area located in the center of the back of the eye on the retina. The macula contains blood vessels and nerve fibers. The retina contains many specialized cells called photoreceptors that sense light coming into the eye, convert light into electrical messages, and send them to the brain through the optic nerve. They allow the brain to perceive the environment.
The retina contains two types of photoreceptor cells: rod and cones. The rods are located primarily outside of the macula and they allow for peripheral (side) and night vision. Most of the photoreceptor cells inside the macula are the cone cells, which are responsible for perceiving color and viewing objects directly in front of the eye (central vision). If the macula is diseased, as in AMD, color and central vision are altered. There are two different types of AMD: dry AMD and wet AMD.
|
|
Author Info: Maria Basile PhD, Pamela J. Nutting MS, CGC, Thomson Gale, Gale, Detroit, Gale Encyclopedia of Genetic Disorders Part II, 2005 |