Oculocutaneous Albinism Type 4
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Oculocutaneous Albinism Type 4
Oculocutaneous albinism is a form of albinism involving the human eye, eyes (''wikt:oculo-#Prefix, oculo-''), the human skin, skin (''-wikt:cutaneous#Adjective, cutaneous''), and the hair. Overall, an estimated 1 in 20,000 people worldwide are born with oculocutaneous albinism. OCA is caused by mutations in several genes that control the biosynthesis, synthesis of melanin within the melanocytes. Seven types of oculocutaneous albinism have been described, all caused by a disruption of melanin synthesis and all autosomal recessive disorders. Oculocutaneous albinism is also found in non-human animals. Types The following types of oculocutaneous albinism have been identified in humans. See also * Piebaldism * List of skin conditions * List of cutaneous conditions associated with increased risk of nonmelanoma skin cancer References External links Oculocutaneous albinism informationat RareDiseases.org NCBI Genetic Testing Registry
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Albinism
Albinism is the congenital absence of melanin in an animal or plant resulting in white hair, feathers, scales and skin and pink or blue eyes. Individuals with the condition are referred to as albino. Varied use and interpretation of the terms mean that written reports of albinistic animals can be difficult to verify. Albinism can reduce the survivability of an animal; for example, it has been suggested that albino alligators have an average survival span of only 24 hours due to the lack of protection from UV radiation and their lack of camouflage to avoid predators. It is a common misconception that all albino animals have characteristic pink or red eyes (resulting from the lack of pigment in the iris allowing the blood vessels of the retina to be visible), however this is not the case for some forms of albinism. Familiar albino animals include in-bred strains of laboratory animals (rats, mice and rabbits), but populations of naturally occurring albino animals exist in the wi ...
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