Werner syndrome, a rare disease that mimics premature aging
Get to know Werner's syndrome, a rare disease
Aging is a natural process that occurs in the body. Starting from gray hair to decreased organ function. In fact, aging may be caused by a rare disease, not just because of age or exposure to free radicals.
There are genetic diseases that show symptoms such as premature aging. Yes, this disease is called Werner's syndrome (Werner's syndrome).
This disease makes a person experience the aging process quickly. This syndrome is the most common type of progeria.
Progeria or Hutchinson-Gilford Progeria syndrome (HGPS), can usually be detected in infants aged 10 months to 1 year. Meanwhile, Werner's syndrome will only cause symptoms after puberty.
What are the symptoms of Werner's syndrome?
Initially, children with this syndrome can develop like other normal children. However, after puberty, physical changes will occur very quickly.
According to the National Institute of Health, various common symptoms of Werner's syndrome are:
- Small size
- Gray hair and hoarse voice
- The skin becomes thin and hard
- His arms and legs are very thin
- There is abnormal fat accumulation in several parts of the body
- The nose becomes sharp like a bird's beak
In addition to physical changes, people with this syndrome will also experience health problems that generally affect the elderly, such as:
- Cataracts with both eyes
- Type 2 diabetes and skin ulcers
- atherosclerosis
- Bone loss (osteoporosis)
- In some cases, it can cause cancer
People with Werner's syndrome can live on average until the late 40s or early 50s. In general, death is caused by atherosclerosis and cancer.
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