that is lack of pigmentation on the skin (melanin). for more information visit the related links box below for the wikipedia article on albinism
differentiate melanin melanocytes and albinism
albinism is a genetic condition where the body does not produce melanin pigment.
No, albinism is an irreversible condition.
Albinism
Albinism occurs equally in both males and females. It is a genetic condition that can affect individuals of any gender.
melanin or eumelanin
Albinism is not a dominant trait; it is a recessive genetic condition caused by mutations in genes responsible for melanin production. Both parents can be carriers of the recessive allele for albinism, meaning they have normal pigmentation but can pass the allele to their child, resulting in the child having albinism.
I think albinism still exists I have heard of some cases about it. Albinism is an inherited condition that is present at birth. Read more at: http://www.answers.com/topic/albinism == Albinism results from the inheritance of recessive alleles. The condition is known to affect mammals (including humans), fish, birds, reptiles and amphibians. 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 genes that are passed on from both parents, although some rare forms are inherited from only one parent.
Genetics play a significant role in the inheritance and manifestation of albinism. Albinism is a genetic condition that is inherited when a person receives two copies of a recessive gene that causes a lack of melanin production in the body. This lack of melanin leads to the characteristic features of albinism, such as pale skin, hair, and eyes. The specific genes involved in albinism can vary, but the condition is generally passed down from parents to their children through genetic inheritance.
Albinism is a genetic condition characterized by a lack of pigmentation in the skin, hair, and eyes. People with albinism often have pale skin, white or light hair, and light-colored eyes. This condition results from a deficiency in melanin production.
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.
Albinism is the congenital absence of melanin in the dermis. Albinism is an inherited condition resulting from the combination of recessive alleles passed from both parents of an individual.This condition is known to affect mammals, fish, birds, reptiles, and amphibians.