How many people in the world have Werner syndrome?

How many people in the world have Werner syndrome? In the United States, it is estimated that about 1 in 200,000 people has Werner syndrome. Worldwide, the prevalence is estimated to be 1 in 380,000

How many people in the world have Werner syndrome?

In the United States, it is estimated that about 1 in 200,000 people has Werner syndrome. Worldwide, the prevalence is estimated to be 1 in 380,000 to 1 in 1,000,000.

Is Werner syndrome inherited?

Werner syndrome is inherited in an autosomal recessive pattern.

Why might Werner syndrome increase the chance of getting cancer?

People with Werner syndrome have an increased risk of cancer, especially thyroid cancer, skin cancer, and sarcoma (a type of bone or soft tissue cancer). Werner syndrome is caused by a mutation (change) in the WRN gene, which makes a protein involved in DNA repair.

Which chromosome does Werner syndrome affect?

However, it was not until 1966 that there was a general consensus on the autosomal recessive mode of inheritance for the syndrome. By 1981, geneticists had located the WRN gene on chromosome 8, leading to its cloning in 1996.

Can Werner syndrome be cured?

People with Werner Syndrome are treated for their various symptoms (cataracts are removed, heart disease is treated, etc.). There is no known cure for the condition.

What is the difference between Werner syndrome and progeria?

These are actually two distinctly different disorders; a major clinical difference is that the onset of the Hutchinson-Gilford syndrome (sometimes called progeria of childhood) occurs within the first decade of life, whereas the first evidence of Werner syndrome (sometimes called progeria of the adult) appears in …

How long do people live with Werner syndrome?

The prognosis is unfavorable. The mean survival for patients with Werner syndrome (WS) is 46 years. Death usually occurs when patients are aged 30-50 years because of atherosclerosis or malignant tumors.

What does mild Noonan syndrome look like?

People with Noonan syndrome have distinctive facial features such as a deep groove in the area between the nose and mouth (philtrum ), widely spaced eyes that are usually pale blue or blue-green in color, and low-set ears that are rotated backward.