What is Werner's syndrome?

Werner syndrome is a recessive autosomal disorder characterized by premature aging. Prigeria refers to a group of premature aging diseases such as Werner syndrome. Werner syndrome is sometimes also classified as a progeroid syndrome and is caused by a inherited mutation of a gene affecting the 8. Chromosome. Werner's syndrome is a very rare condition that has been reported only in a small percentage of the world's population.

Werner's syndrome is named for Otto Werner, a German scientist who originally described the syndrome in his 1904 doctoral thesis. In 1997, the gene responsible for Werner syndrome was identified as RecQL2. Research has shown that the syndrome is the most common in the Asian part of the population, because a higher percentage of reported cases came from Japan than from any other country.

Individuals with Werner syndrome usually develop at normal speed until they reach puberty. After the advent of puberty they tend to age and development, including growth frauds that experience normalMake -up teenagers are missing. This usually leads to shorter than normal characters in those who suffer from Werner syndrome. Other symptoms that are usually present in individuals affected by Werner syndrome include timely loss and grayness of hair, premature skin reinforcement and cataracts in both eyes.

Patients with Werner syndrome also tend to use diseases and disorders that are usually associated with aging, including various cancer, atherosclerosis and heart disease and sometimes diabetes mellitus. Werner patients can live by the end of the 1940s or in the 1950s, but generally suffer from diseases that lead to death earlier in life than usual.

Although there is no cure for Werner syndrome, patients suspect that they have a condition, are tested on the Mutatued Gen for correct control of health conditions usually affecting patients. Werner's syndrome is extremelyUnusual and usually does not apply to problems, but those who suspect that they can be bearers of a recessive gene can participate in genetic counseling before reproduction.