Wiedemann Rautenstrauch Syndrome
National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Wiedemann Rautenstrauch Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- neonatal progeroid syndrome
- neonatal pseudo-hydrocephalic progeroid syndrome of WRS
- Rautenstrauch-Wiedemann syndrome
Wiedemann-Rautenstrauch syndrome (WRS), also known as neonatal progeroid syndrome, is a very rare genetic disorder characterized by an aged appearance at birth (old man look) growth delays before and after birth (prenatal and postnatal growth retardation), and deficiency or absence of the layer of fat under the skin (subcutaneous lipoatrophy). It is anticipated that most individuals with WRS have decreased life expectancy. There are few individuals who have lived well in to the teens and afew still live in their 20s. WRS is inherited as an autosomal recessive trait, as several pairs of siblings have been reported in families with unaffected parents.
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NIH/National Institute of Neurological Disorders and Stroke
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Progeria Research Foundation, Inc.
- P.O. Box 3453
- Peabody, MA 01961-3453
- Tel: (978)535-2594
- Fax: (978)535-5849
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- Website: http://www.progeriaresearch.org
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It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
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Last Updated: 1/7/1970
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