WS — Werner Syndrome

It is feasible that the main title of the report Werner Syndrome is not the name you expected. Please check the synonyms providing to find the alternative name(s) and also disorder community(s) covered by this report.


  • Progeria of Adulthood
  • WNS
  • WS
  • Atypical Werner Disorder

Condition Communities

  • None

General Discussion
Werner Disorder is an unusual modern problem that is characterized by the look of abnormally sped up growing old (progeria). Although the disorder is usually recognized by the 3rd or fourth decades of life, particular particular searchings for are present beginning throughout adolescence and early adulthood.

Individuals with Werner Syndrome have an abnormally slow-moving growth rate, as well as there is cessation of development at puberty. As a result, influenced people have brief stature and reduced weight relative to elevation. By age 25, those with the problem commonly experience early graying (canities) and early loss of scalp hair (alopecia). As the condition progresses, extra abnormalities include loss of the level of fat below the skin (subcutaneous adipose tissue); serious losing (degeneration) of muscle mass cells in particular areas of the physical body; as well as degenerative skin modifications, particularly in the facial area, the upper arms as well as hands, and also the lower legs as well as feet (distal extremities). Because of degenerative modifications impacting the face location, individuals with Werner Disorder might have uncommonly noticeable eyes, a beaked or pinched nose, and/or various other unique facial abnormalities.

Werner Disorder might also be characterized by development of an unique high-pitched voice; eye irregularities, consisting of premature clouding of the lenses of the eyes (reciprocal senile cataracts); and specific endocrine problems, such as impaired performance of the ovaries in ladies or testes in men (hypogonadism) or unusual manufacturing of the hormonal agent insulin by the pancreas and resistance to the results of insulin (non-insulin-dependent diabetic issues mellitus). Furthermore, individuals with Werner syndrome might establish dynamic thickening and loss of suppleness of artery wall surfaces (arteriosclerosis). Affected blood vessels typically include the arteries that move oxygen-rich (oxygenated) blood to heart muscle (coronary arteries). Some impacted people may additionally be vulnerable to establishing particular benign (noncancerous) or malignant tumors. Progressive arteriosclerosis, hatreds, and/or connected irregularities could result in potentially dangerous problems by around the fourth or 5th decade of life. Werner syndrome is acquired as an autosomal recessive attribute.

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