Albinism research

Albinism research, Individuals with oculocutaneous albinism, type 1 (oca1) have white hair, very pale skin, and light-colored irises because they have none, or very little, of the pigment melanin in their skin, hair, and eyes affected individuals have impaired eyesight and a substantially increased risk of skin cancer.

Albinism is a syndrome in which the albinos (people who have albinism) do not have color in their skin, eyes or hair they lack the pigment melanin which gives you color in those areas people with albinism inherited an altered copy of a gene from their parents the gene does not work as it should. This database includes mutations associated with all major known forms of oculocutaneous and ocular albinism the albinism database is part of the cell research. Page:1 albinism is a very serious disease that could end up in death albinism is a recessive inherited defect in melanin, which is metabolism in which pigment is.

Purpose of study: this research study is being conducted to understand how retinal development is altered in individuals with albinism what is albinism. Medical research for albinism including cure research, prevention research, diagnostic research, and basic research.

 · albinism is a group of inherited disorders that results in little or no production of the pigment melanin, which determines the color of the skin, hair and eyes melanin also plays a role in the development of certain optical nerves, so all forms of albinism cause problems with the development and function of the eyes.

  • New research unlocks a mystery of albinism december 16, 2014 media contact: david orenstein 401-863-1862 a team led by brown university biologists has discovered the way in which a specific genetic mutation appears to lead to the lack of melanin production underlying a form of albinism.
  • Resources are also available for those doing research on albino people noah is a volunteer organization which provides people with albinism.

How can the answer be improved. Oculocutaneous albinism (oca) is a heterogeneous group of autosomal recessive disorders resulting from mutations of the tyrosinase (tyr) gene and presents with.

Albinism research
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