Neonatal progeroid syndrome
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Wiedemann–Rautenstrauch syndrome (WRS) is a premature aging syndrome in which features of human aging are apparent at birth, including larger than nomal sized head; prominent scalp veins; triangular, aged face; wrinkled skin; and decreased fat under the skin.[2] This differentiates WRS from other premature aging syndromes such as Hutchinson–Gilford progeria syndrome (HGPS) (more commonly called progeria) in which characteristics of premature aging typically become apparent some time after birth.[1] Although the exact cause of WRS is unknown, it is believed to be genetic and inherited in an autosomal recessive fashion.[1] Treatment is based on the individual's specific symptoms.
References
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Arboleda G, Ramirez N, Arboleda H. The neonatal progeroid syndrome (Wiedemann-Rautenstrauch): a model for the study of human aging?. Exp Gerontol. 2007 Oct;42:939-943;
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Pivnick EK. NORD Guide to Rare Disorders. In: . Neonatal Progeroid Syndrome. Philadelphia:Lippincott Williams & Wilkins; 2003:
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- More Detailed Information (Found: 3 Resources)
Links where you can find more general information, comprehensive resources, selected full text journal articles, and news updates
- General
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The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
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The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Neonatal progeroid syndrome. Click on the link to go to OMIM and review these resources.
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PubMed is a searchable database of medical literature and lists journal articles that discuss Neonatal progeroid syndrome. Click on the link to view a sample search on this topic.
- Support Groups (Found: 6 Resources)
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Progeria Research Foundation, Inc.
P.O. Box 3453
Peabody, MA 01961-3453
Telephone: 978-535-2594
Fax: 978-535-5849
E-mail: info@progeriaresearch.org
Web site: http://www.progeriaresearch.org
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MUMS National Parent to Parent Network puts parents in touch with other parents who have children with this condition or similar symptoms.
MUMS National Parent to Parent Network
150 Custer Court
Green Bay, Wisconsin 54301-1243
Toll-free: 877-336-5333 (Parents only please)
Telephone: 920-336-5333
Fax: 1-920-339-0995
E-mail: mums@netnet.net
Web site: http://www.netnet.net/mums/
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RareShare is an online social hub dedicated to patients, families and healthcare professionals affected by rare medical disorders. Click on RareShare to learn more.
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