Most species contain albinos. It's not even special to humans, much less a specific race. In short, all races.
*affected
Chromosome 9.
man get out of here!!!!!!!
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Individuals with albinism typically have a recessive genetic trait, meaning they must inherit two copies of the albinism gene (aa) to express the condition. Therefore, the possible genotypes of the parents could be either both carriers (Aa), one carrier and one affected (Aa and aa), or both affected (aa). If both parents are carriers, there is a 25% chance for each child to be affected by albinism.
same as rest of population
If both parents carry the gene for albinism, which is an autosomal recessive disorder, there is a 25% chance their child will be affected by albinism, a 50% chance the child will be a carrier like the parents, and a 25% chance the child will neither have albinism nor be a carrier. Therefore, there is a 75% chance that their child will not have albinism, either being a carrier or completely unaffected.
Albinism affects genes responsible for producing melanin, the pigment that gives color to skin, hair, and eyes. Mutations in these genes can result in a lack of melanin production, leading to the characteristic features of albinism such as pale skin, light hair, and vision problems.
Estimating the exact number of albinos worldwide is challenging due to varying definitions and reporting standards. However, it is estimated that about 1 in 17,000 to 1 in 20,000 individuals are affected by albinism globally. This suggests that there could be approximately 250,000 to 300,000 people with albinism worldwide, though this number may vary by region and population.
No, albinism does not inherently cause sterility. Individuals with albinism can reproduce, as their condition primarily affects pigmentation due to genetic mutations rather than reproductive capabilities. However, some health issues associated with albinism, such as vision problems, may impact their reproductive choices or opportunities. Overall, fertility is not directly affected by albinism itself.
Albinism is not a disease. People with albinism have little or no pigment in their eyes, skin, or hair. They have inherited altered genes that do not make the usual amounts of pigmment called melanin. Albinism affects people from all races. Most children with albinism are born to parents who have normal hair and eye color for their ethnic backrounds. There are different types of albinism, but all forms are associated with vision problems.
Albinism is a genetic condition caused by mutations in genes responsible for the production of melanin, the pigment that gives color to skin, hair, and eyes. The most common types of albinism are Oculocutaneous albinism (OCA) and Ocular albinism (OA), each associated with different genetic mutations. Individuals with albinism typically have very light skin and hair, and may experience vision problems due to a lack of pigment in the eyes. The condition is inherited in an autosomal recessive manner, meaning that both parents must carry the mutated gene for a child to be affected.