Were delighted youre doing a report on albinism, one of the
most interesting, yet often misunderstood, genetic phenomena. The majority
of the materials NOAH publishes about albinism are on this web site. Feel
free to print and circulate any material. We ask, however, that you leave
the material in tact with the appropriate copyright information.
What
is albinism?
Where can I find facts about albinism?
What do people with albinism look like?
What is it like to have albinism?
Where can I find hard-core scientific
information about albinism?
Who discovered albinism?
What is the chromosomal location for
genes associated with albinism?
What other websites discuss albinism?
I Read EVERYTHING here and I still have
questions about albinism. How can I contact NOAH?
What is albinism?
Albinism is a group of genetic conditions that causes a lack of pigment. It
can effect only the eyes (ocular albinism) or both the eyes and skin (oculocutaneous
albinism). Most types of albinism are inherited when an individual receives
the albinism gene from both parents. The exception is one type of ocular albinism,
which is passed on from mothers to their sons.
For more information on the genetics of albinism, see the NOAH
Information Bulletin What is Albinism
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Where can I find facts about albinism?
See NOAHs information
Bulletins
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What do people with albinism look
like?
While most people with albinism have very light skin and hair, not all do.
In less pigmented types of oculocutaneous albinism, (the type of albinism that
affects both the skin and the eyes), hair and skin are cream-colored. In types
with slight pigmentation, hair appears more yellow or red-tinged People with
ocular albinism (albinism that only affects the eyes) usually have normal or
only slightly lighter than normal physical appearance. A common myth is that
by definition people with albinism have red eyes. In fact there are different
types of albinism, and the amount of pigment in the eyes varies. Most individuals
with albinism have blue eyes. Some have hazel or brown eyes. See NOAHs
Information Bulletin What is Albinism for more information about how albinism
affects a persons appearance You can see pictures of people with albinism
at Positive Exposure, a photo
project dedicated to celebrating the beauty of people with albinism.
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What is it like to have albinism?
Visit the Albinism Online Community. Youll
find several forums where people share experiences and ask questions. Among
the forums are specific forums for Teens with Albinism, Adults with Albinism,
and People of Color with albinism. You can gain a lot of insight on what it
is like to live with albinism just by reading some of the posts. Please read
before you post..
One NOAH publications is NOT available on this site also discuss what life
is like for people with albinism. Albinism, the People the Challenge is a video.
NOAH offers for a nominal fee. Call NOAH toll-free at 1-800-473-2310, or email
NOAH, to order a copy. Once you have completed your research, why not donate
the video to your local library so others may learn about albinism?
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Where can I find hard-core scientific
information about albinism?
Visit the International Albinism Center Web Site at
http://albinism.med.umn.edu/
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Who discovered albinism?
We consulted the experts and this was the answer we received."I believe
that albinism has been in "literature" since the beginning of medical
literature. There have been several Greek and Roman authors (Plinius Secundus
the elder and Aulus Gellius for example) that have described albinism in man.
I do not believe that anybody discovered albinism. Tyrosinase deficiency in
animals was first demonstrated in 1904. The first accurate scientific paper
written about albinism was by Sir Archibald Garrod in 1908."
- William S. Oetting, Ph.D.
Department of Medicine - Genetics
University of Minnesota
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What is the chromosomal location
for genes associated with albinism?
For the most current information please see http://albinismdb.med.umn.edu/
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What other websites discuss albinism?
Please see our Related Links section
I Read EVERYTHING here and I still
have questions about albinism. How can I contact NOAH?
E-mail NOAH or call NOAH toll-free
at 1-800-473-2310.
NOAH is a volunteer organization for persons and families involved with
the condition of albinism. It does not diagnose, treat, or provide genetic
counseling. It is involved in self-help, while trying to promote research
and education.
Copyright 1995-2002 The National Organization
for Albinism and Hypopigmentation