Is also called as achromia, achromasia, or achromatosis. Albinism is a rare group of genetic disorders that cause the skin, hair, or eyes to have little or no colour. Albinism is also associated with vision problems. Albinism is caused by a defect in one of several genes that produce or distribute melanin (natural pigment). The defect may result in the absence of melanin production, or a reduced amount of melanin production. Albinism is inherited and requires the defective gene to be passed down by both parents.
Symptoms: They include Absence of colour in the hair, skin, or iris of the eye, Lighter than normal skin and hair, Patchy, missing skin colour. Many forms of albinism are associated with the following symptoms: Crossed eyes (strabismus), Light sensitivity (photophobia), Rapid eye movements (nystagmus), Vision problems, or functional blindness.
Because albinism is a genetic disorder, treatment is limited. Therefore treatment involves protecting the skin and eyes from the sun: Reduce sunburn risk by avoiding the sun, using sunscreen, and covering up completely with clothing when exposed to the sun. We should use Sunscreen to have a high sun protection factor (SPF), Sunglasses (UV protected) may relieve light sensitivity.The approximate Albinism Incidence in Western Europe of France was found to be 3,021.