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In this case, the one normal gene provides enough information in its cellular blueprint to make some pigment, and the child will have normal skin and eye color. About one in 70 people are albinism carriers, with one flawed gene but no symptoms; they have a 50% chance of passing the albinism gene to their child.

However, if both parents are carriers with one flawed gene each, they have a 1 in 4 chance of passing on both copies of the flawed gene to the child, who will have albinism.

In its most severe form, hair and skin remain pure white throughout life.

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Many types of albinism exist, all of which involve lack of pigment in varying degrees.

The condition, which is found in all races, may be accompanied by eye problems and may lead to skin cancer later in life.

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Albinism is a rare disorder found in fewer than five people per 100,000 in the United States and Europe.