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Albinism
Websites
An organization where people with albinism, their families and those that work with them can get information, ask questions and share their experiences.
http://www.albinism.org
Information on albimism and how it affects a boy.
http://www.stumm.co.uk/
Explore the mythology of albinism.
http://www.lunaeterna.net/popcult/
An article about albinism as well as ocular albinism, related conditions, testing and who treats this.
http://www.eyemdlink.com/Condition.asp?ConditionID=59
Information and resources about the syndrome and albinism.
http://www.medhelp.org/web/hpsn.htm
Voluntary organisation that aims to provide information, advice and support, for people with Albinism.
http://www.albinism.org.uk/
Adam.com looks at this disorder and its alternative names. A definition and a look at the causes, incidence and risk factors.
http://www.nlm.nih.gov/medlineplus/ency/article/001479.htm
Dedicated to curing childhood hereditary blindness, including ocular albinism and other related genetic vision disorders.
http://www.visionofchildren.com/
At the University of Minnesota a team of dedicated research professionals interested in understanding the basis of albinism in humans. Facts about this disorder as well as glossary of terms provided.
http://albinism.med.umn.edu/
Scientific society devoted to those of us interested in various aspects of pigment cells.
site exerpt
Welcome to the PanAmerican Society for Pigment Cell Research Society is a very interactive one, meeting on an annual basis, and is composed of clinicians, developmental biologists, biochemists, immunologists, cell biologists, molecular biologists, chemists and physicists, among other disciplines. Look at the PASPCR Information Page for more information on...