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Top/Health/Conditions and Diseases/Rare Disorders/Progeria |
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Progeria : |
| Progeria is a rare genetic condition characterized by an appearance of accelerated aging in children. Its name is derived from the Greek and means "prematurely old." The classic type is the Hutchinson-Gilford Progeria Syndrome which was first described in England in 1886 by Dr. Jonathan Hutchinson and again in 1886 and 1904 by Dr. Hastings Gilford. |
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10 web sites matced for Progeria |
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Hutchinson-Gilford Progeria Syndrome (HGPS) Resource Page
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Provides an overview of the disease as well as links to resources.
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University of Washington: Werner Syndrome
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Images of persons with this disease and diagnostic criteria for WRN and contact information for a central repository of WS data and research and materials.
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Progeria Research Foundation, Inc.
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Medical research, education, support, and fundraising for this "pre-mature aging" disease.
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Online Mendelian Inheritance in Man - Progeria
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Progeria medical database resource for textual information, pictures, and reference information.
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Progeria Family Circle
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Overview of the rare disorder, symptoms, and experiences of children with Progeria and their families.
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NORD: Progeria, Hutchinson Gilford
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Outlines the symptoms and lists related organizations.
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NORD: Werner Syndrome
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Offers alternative names, a general discussion and further resources.
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Progeria Project Foundation
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A group concerned about the well-being and quality of life for Progeria children and their families.
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NCBI: Genes and Diseases
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Provides a short descriptions of the inherited disorder, Werner syndrome.
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Progeria.ca: Too Young to be Old
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Information and community portal. Includes explanation of progeria, book list, and a forum.
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