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Werner Syndrome (WS) (also known as "Adult progeria"^[1]:573) is a very rare, autosomal recessive^[2] disorder characterized by the appearance of premature aging.^[3]

Werner's syndrome more closely resembles accelerated aging than any other segmental progeria. For this reason, Werner syndrome is often referred to as a progeroid syndrome, as it partly mimics the symptoms of Progeria.

[edit] Pathophysiology

The defect is on the WRN gene that codes DNA helicase and it is located on the short arm of the 8th chromosome. The disorder is directly caused by shorter-than-normal length telomere maintenance. As a result DNA replication is impaired.

[edit] Symptoms

Individuals with this syndrome typically develop normally until they reach puberty. Following puberty they age rapidly, so that by age 40 they often appear several decades older. The age of onset of Werner syndrome is variable, but an early sign is the lack of a teenage growth spurt, which results in short stature. Other signs and symptoms appear when affected individuals are in their twenties or thirties and include loss and graying of hair, hoarseness of the voice, thickening of the skin, and cloudy lenses (cataracts) in both eyes. Overall, people affected by Werner syndrome have thin arms and legs and a thick torso.

Affected individuals typically have a characteristic facial appearance described as "bird-like" by the time they reach their thirties. Patients with Werner syndrome also exhibit genomic instability, hypogonadism, and various age-associated disorders; these include cancer, heart disease, atherosclerosis, diabetes mellitus, and cataracts. However, not all characteristics of old-age are present in Werner patients; for instance, senility is not seen in individuals with Werner syndrome. People affected by Werner syndrome usually do not live past their late forties or early fifties, often dying from the results of cancer or heart disease.

[edit] Genetics

Werner syndrome has an autosomal recessive pattern of inheritance.

Werner syndrome is an autosomal recessive disorder.^[2] The gene associated with Werner Syndrome lies on chromosome 8 in humans.^[4]

[edit] History

Werner's syndrome is named after Otto Werner,^[5] a German scientist, who, as a student, described the syndrome as part of his doctoral thesis in 1904.

[edit] See also

• Accelerated aging disease
• Biogerontology
• Cockayne syndrome
• DNA repair
• Degenerative disease
• Genetic disorder
• Life extension
• Progeria
• Senescence
• Xeroderma pigmentosum

[edit] References

[edit] External links

This article incorporates public domain text from The U.S. National Library of Medicine

• Werner syndrome at libero.it
• DNA Repair at rcn.com
• Segmental Progeria at benbest.com
• WRN at the GenAge database.
• werner at NIH/UW GeneTests
• 00421 at CHORUS