About Albinism

Albinism is an inherited condition. People with albinism have little or no melanin, which is a chemical that colors our skin, eyes and hair. Therefore, people with albinism lack pigmentation in the skin, eyes and hair. Albinism affects people of all races and ethnicities and is much more common than you may think. In fact, one out of every 17,000 people worldwide has some form of albinism. In some populations, it occurs in one out of every 200 births.

Most forms of albinism are recessive, which means that a child inherits one abnormal gene from each parent. Most children with albinism are born to parents with normal pigmentation. These parents — like one in every 75 people — are carriers for albinism. A carrier is someone who has one abnormal gene and one that functions normally. Because the functional gene overrides the abnormal one, these people do not have albinism themselves. However, they are still able to pass the abnormal gene on to their child.

Although people with albinism always have problems with vision, the degree varies greatly. Some are legally blind, while others have vision that is good enough to drive a car. Most are able to read without using Braille.

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  • Useful Links for Albinism: General Medical Information About Albinism International Albinism Center Wikipedia's Albinism Page Albinism's Eye Conditions eMedicine Albinism Information Kid's Health Skin Cancer Information Medical Information About Albinism Sub-Types Griscelli Syndrome Information Chediak-Hagashi Information HPS Information OCA1a OCA 1b OCA2 OCA4 HPS Other Albinism-Related Groups Albinism Through the Eyes...