LYCOS RETRIEVER 
Albinism: Parents
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Albinism is an inherited disorder. A person with albinism has received an abnormal gene from his or her parents. Most children with albinism are born to parents with normal melanin production and no symptoms of albinism.
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Albinism is a autosomal recessive disease, which means that a person must have two copies of the defective gene to exhibit symptoms of the disease. The child therefore inherits one defective gene responsible for making melanin from each parents. Because the task of making melanin is complex, there are many different types of albinism, involving a number of different genes.
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Albinism is hereditary; it is not an infectious disease and cannot be transmitted through contact, blood transfusions, or other vectors. The principal gene which results in albinism prevents the body from making the usual amounts of the pigment melanin. Most forms of albinism are the result of the biological inheritance of genetically recessive alleles (genes) passed from both parents of an individual, though some rare forms are inherited from only one parent. There are other genetic mutations which are proven to be associated with albinism. All alterations... lead to changes in melanin production in the body.[1][2]
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Albinism occurs as a result of altered genes, which are in most cases inherited from parents. Albinism appears in different forms and may be inherited by one of several modes: autosomal recessive, autosomal dominant, or X-linked.
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Albinism is mostly a recessively inherited disease, which means that you have inherited two albinism genes (one from each parent). If your parents are only carriers of albinism (each having one albinism gene and one normal gene) they will have enough genetic information to make normal pigment and will not show any signs of albinism.
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