Werner syndrome - Skin
The disease has autosomal recessive inheritance and is markedly increased in the Japanese, due to a founder mutation in that population, and in Sardinia. All races and ethnic groups are affected, and there is not a significant difference in incidence between sexes. The affected gene WRN is a helicase (RECQL2) involved with DNA replication, recombination, and repair. There are dozens of different causative mutations of WRN, often causing a truncated protein.
During childhood, the patient's voice may be high-pitched or hoarse, but except for familial cases, this diagnosis is rarely made before the third or fourth decade.
In the third decade (twenties), greying of the hairs (often at the temples) may be the first sign, followed by generalized hair loss, localized hyperkeratosis over boney prominences, and soft tissue atrophy (on the extremities but not the trunk). Malignancies begin to occur.
In the fourth decade (thirties), bilateral postcortical and subcapsular cataracts, testicular atrophy, early menopause, premature atherosclerosis, skin ulcers, and diabetes occur.
Malignancies begin to occur during the third decade and increase during the rest of the patient's life. Tumors in WS often occur at an earlier age than the same tumor in the general population. Frequent neoplasms, often of mesenchymal tissue origin, include thyroid carcinomas, various forms of melanoma (mucosal and acral lentiginous melanoma, more common in the Japanese population), meningiomas, soft tissue sarcoma, hematologic and lymphoid malignancies, and osteosarcomas. Cancer risk for most common malignancies is increased in WS.
Major (cardinal) signs include:
- Bilateral cataracts
- Short stature
- Premature greying, thinning, and loss of hair
- Skin changes including tight skin (sclerosis), atrophic skin, pigmentary changes, ulceration, hyperkeratosis, regional subcutaneous atrophy and sclerosis ("birdlike" facies)
For more information, see OMIM.
E34.8 – Other specified endocrine disorders
51626007 – Werner syndrome
- Progeria – Starts in the first decade, often the first years of life, and signs of premature aging are very prominent before the age of 10. Most patients have abnormal lamin genes.
- Lamin heterozygous disease – Very similar to WS but starts in the early twenties and has an accelerated course. Patient usually does not have diabetes or bilateral cataracts.
- Mandibuloacral dysplasia – No cataracts. Recessive. Starts in childhood.
- Rothmund-Thomson disease – A defect in the RecQ helicase gene. Onset in childhood is contrasted with WS.
- Diabetes – Sclerotic changes with mucopolysaccharide deposition.
- Scleroderma and morphea – Without the accelerated aging associations.
- Vascular disease with leg ulcers – Buerger disease (thromboangiitis obliterans).
- Pseudoxanthoma elasticum (PXE) – Vascular disease; has lax skin, not sclerosis.
- Calcinosis cutis – Without premature aging.
- Familial partial lipodystrophy – Without premature aging.