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Описание: Dystrophic Epidermolysis Bullosa Research Association. A voluntary, non-profit organization dedicated to creating awareness and providing support for families affected by Epidermolysis Bullosa (EB). Includes treatment and care ...
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The Dystrophic Epidermolysis Bullosa Research Association of America (debra), the only national non-profit dedicated to funding research and providing services and ...
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Information, mailing list, pictures, and help for new parents.
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An organization where people with albinism, their families and those that work with them can get information, ask questions and share their experiences.
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Features organization background, information about the disorder, fundraising and research details, and news.
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The EBMRF is a volunteer, non-profit Foundation dedicated to helping medical scientists learn more about EB, its causes, the development of successful treatments ...
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A small group of relatives and friends of EB patients founded DEBRA Canada in 1998. That informal group has evolved into a Board of 10 people who meet monthly to ...
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Progeria: A very rare terminal condition. From the Greek meaning "prematurely old". Characterized by an appearance of accelerated aging. This Web Site is ...
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Includes downloadable articles and booklets as well as links of interest. Also offers password-protected forums for professionals.
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