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Newly published research provides the first demonstration of how a genetic mutation associated with a common form of albinism leads to the lack of melanin pigments that characterizes the condition.
The discovery could inspire new ideas for treating albinism, said elena oancea, assistant professor of medical science and senior author of the paper published in the journal elife.
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Although preponderance data are insufficient and further epidemiological research is needful, the number of people living with albinism in Africa is likely to be as broad as tens of thousands.
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Where did the research on albinism take place?
PROVIDENCE, R.I. [Brown University] — Newly published research provides the first demonstration of how a genetic mutation associated with a common form of albinism leads to the lack of melanin pigments that characterizes the condition.
What is new research on albinism at Brown University?
New research unlocks a mystery of albinism. In the new research a team led by Brown University biologists Nicholas Bellono and Elena Oancea shows that the protein is necessary for the proper functioning of an ion channel on the melanosome organelle, the little structure in a cell where melanin is made and stored.
Is there a way to unlock the mystery of albinism?
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.
How many people in the world have albinism?
About 1 in 40,000 people worldwide have type 2 oculocutaneous albinism, which has symptoms of unsually light hair and skin coloration, vision problems, and reduced protection from sunlight-related skin or eye cancers.
Last Update: Oct 2021
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