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Synonyms: adult premature ageing syndrome, adult progeria
Werner's syndrome (WS) is an extremely rare, autosomal recessive, systemic disease which is associated with features of premature aging and cancer predisposition. The syndrome is named after C. W. Otto Werner, a German physician (1879-1936).
Interest in Werner's syndrome (WS) is fuelled in part by the observation that transcription aberrations in WS are similar to those found in normal ageing. In WS, the gene defect is known to affect WRN (found on chromosome 8) encoding Werner protein, a nuclear protein with helicase and exonuclease activity important in maintaining and repairing DNA, particularly where double-strand breaks occur.[2, 3] WRN gene mutations encode an abnormally shortened Werner protein.
More than 50 different disease-causing mutations in the WRN gene have been identified in WS patients.
- It is extremely rare, with only approximately 1,300 cases reported worldwide since 1916, with 1,000 of those coming from Japan.
- A prevalence of 1/200,000 US population is contrasted with 1/20-40,000 Japanese population (ie 10-20 x more common).
- In Japan the frequency of heterozygote carriers of the condition within the general population is estimated as 1/180.
- Typically, individuals grow normally until puberty.
- The first symptom is the lack of a teen growth spurt.
- Early findings (observed in the 20s) are loss and greying of hair, hoarseness and scleroderma-like skin changes.
- This is followed (typically in the 30s) by bilateral cataracts, type 2 diabetes mellitus, hypogonadism, refractory skin ulcers and osteoporosis.
- Most will present to dermatologists or ophthalmologists in the first instance.
Typical signs and symptoms
Suggested diagnostic criteria:
- Bilateral cataracts.
- Characteristic skin: tight, atrophic, pigmentary changes, ulceration, hyperkeratosis.
- 'Bird-like' facies.
- Short stature.
- Premature greying and/or balding.
Other signs and symptoms
- Type 2 diabetes mellitus.
- Hypogonadism and decreased fertility.
- Osteosclerosis of distal phalanges of fingers and/or toes.
- Soft-tissue calcification.
- Premature arteriosclerosis.
- Neoplasms: mesenchymal (sarcomas), unusual or multiple types or sites.
- High-pitched, squeaky or hoarse voice.
- Flat feet.
- Atypical Werner's syndrome (WS) - small subset with normal WRN protein. Earlier age of onset and faster progression compared with classic WS.
- Hutchinson-Gilford progeria syndrome most closely resembles WS. Neonates with WS appear normal but fail to thrive during their first year, with connective tissue abnormalities becoming apparent in the second and third year, and death usual between 6-20 years.
- Early-onset type 2 diabetes mellitus with secondary vascular and skin complications.
- Myotonic dystrophy - in view of the young adult-onset cataracts - but other features are different and onset is usually in adulthood.
- Scleroderma, mixed connective-tissue disorders, lipodystrophy and Charcot-Marie-Tooth syndrome have some skin features similar to WS.
- Urinary and serum hyaluronic acid is increased in most individuals.
- Sequence analysis of the WRN coding region detects mutations in both alleles for approximately 90%.
- Western blot - usually absent Werner protein.
Werner's syndrome (WS) is associated with several diseases of old age including:
- Myocardial infarction.
- Cancers - x 10 risk of epithelial cancers and mesenchymal sarcomas compared with the general population.
- Cerebral infarction.
- Diabetes mellitus.
Early recognition of the syndrome is helpful, as screening for malignancies and associated diseases such as diabetes may then be performed on a regular basis.
There is no specific treatment available for Werner's syndrome (WS), although surgical intervention and hyperbaric oxygen therapy may be of use in the treatment of refractory skin ulcers.
- Treatment of diabetes - glitazones are thought to be particularly effective.
- Cholesterol lowering where lipid profile is abnormal.
- Standard treatments for malignancies and ischaemic heart disease.
- Preliminary mouse studies suggest vitamin C supplementation may be beneficial.
- Specific surgical procedures may be required to treat complications such as cataracts and contractures.
Fertility is much reduced but there are recorded instances of individuals of both sexes having children.
- Obligate carrier status of all affected individual's children.
- For siblings of an affected individual, there is a 1 in 4 risk of having the disease and a 1 in 2 risk of carrier status as a sibling.
- Relatives of affected individuals should have increased cancer surveillance.
The life span of individuals with Werner's syndrome (WS) is reduced. Death occurs on average in the mid-40s, commonly as a result of malignancy or myocardial infarction.
Prenatal screening may be available to parents who are considered at high risk of having an affected child.
Further reading and references
Kyng KJ, Bohr VA; Kyng KJ, Bohr Gene expression and DNA repair in progeroid syndromes and human aging. Ageing Res Rev. 2005 Nov
Lan L, Nakajima S, Komatsu K, et al; Accumulation of Werner protein at DNA double-strand breaks in human cells. J Cell Sci. 2005 Sep 15118(Pt 18):4153-62. Epub 2005 Sep 1.
Muftuoglu M, Oshima J, von Kobbe C, et al; The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis. Hum Genet. 2008 Sep 23.
Yamamoto K, Imakiire A, Miyagawa N, et al; A report of two cases of Werner's syndrome and review of the literature. J Orthop Surg (Hong Kong). 2003 Dec11(2):224-33.
Nakura J, Wijsman EM, Miki T, et al; Homozygosity mapping of the Werner syndrome locus (WRN). Genomics. 1994 Oct23(3):600-8.
Gene review; Werner syndrome. Last updated 2007 funded by NIH
Hattori S, Kasai M, Namatame T, et al; Pioglitazone treatment of insulin resistance in a patient with Werner's syndrome. Diabetes Care. 2004 Dec27(12):3021-2.
Leistritz DF, Hanson N, Martin GM, et al; Werner Syndrome
Janniger CK et al; Werner Syndrome, Medscape, Jan 2010
Hi all, I am a newbie here. I am 37 and 11 weeks pregnant with my second baby. I was 28 at the time of first delivery and haven't done any genetic testing at that time. But I know the risk factors...Zaynah
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