Albinism is an example of a genetic condition caused by mutations that affect the production of melanin, the pigment responsible for skin, hair, and eye color. It is inherited in an autosomal recessive manner, meaning that an individual must receive two copies of the mutated gene—one from each parent—to manifest the condition. Albinism results in various degrees of pigmentation deficiency, leading to increased sensitivity to sunlight and a higher risk of skin cancer and vision problems.
albinism is common.
Albinism is a rare disorder found in fewer than five people per 100,000 in the United States and Europe. Other parts of the world have a much higher rate; for example, albinism is found in about 20 out of every 100,000 people in southern Nigeria.
What are the demographics of albinism:
Ocular Albinism is a type of albinism that affects mostly vision. It commonly comes with the lack of melanin in the skin that occurs in regular albinism.
Albinism is a congenital disorder.
Albinism is a recessive trait.
Albinism is a recessively inherited disease. People with albinism has inherited 2 albinism genes. They got one gene from each parent.
In the Philippines,A celebrity that has albinism is redford white.
differentiate melanin melanocytes and albinism
Melanism is rarer than Albinism
One example of a disorder that affects physical appearance is albinism. Albinism is a genetic condition characterized by the absence of melanin, which leads to very light skin, hair, and eyes. People with albinism may also have vision problems and be more susceptible to sunburn and skin cancer.
People who have a family history of albinism will be the most likely to get albinism but normal people have a chance of getting it