What is Werner syndrome?
What is Werner syndrome?
Werner syndrome is a rare progressive disorder that is characterized by the appearance of unusually accelerated aging (progeria). Although the disorder is typically recognized by the third or fourth decades of life, certain characteristic findings are present beginning during adolescence and early adulthood.
Why are some people born with thin skin?
Translucent skin is typically genetic, but may be caused by albinism, vitiligo, tinea versicolor, or other conditions.
How do you treat thin skin naturally?
Include plenty of fruits and vegetables, whole grains, and proteins. Vitamin E, found in foods such as almonds and avocados, can also support skin health. The fats in these foods may help to keep the skin supple. Drinking enough water helps to keep the skin hydrated.
Why is my skin so thin and fragile?
Fragile or thin skin that tears easily is a common problem in older adults. Aging, sun exposure and genetics all play a role in thinning skin. Certain medications, such as long-term use of oral or topical corticosteroids, also can weaken the skin and blood vessels in the skin.
What are the symptoms of acrogeria, Gottron type?
Summary Summary. Acrogeria, Gottron type is a premature aging syndrome. Characteristic signs include fragile, thin skin on the hands and feet. Other parts of the body (e.g., face, forearms, and lower legs) are variably affected.
What do you need to know about Gottron syndrome?
General Discussion. Gottron syndrome (GS) is an extremely rare inherited disorder characterized by the appearance of premature aging (progeria), especially in the form of unusually fragile, thin skin on the hands and feet (distal extremities). GS is described as a mild, nonprogressive, congenital form of skin atrophy due to the loss…
Why do people with Gottron syndrome have hollow cheeks?
Gottron syndrome is described as a mild, nonprogressive, congenital form of skin atrophy due to the loss of the fatty tissue directly under the skin (subcutaneous atrophy). This causes the skin to have a dry and transparent appearance. The affected individual is often noted to have hollow cheeks, a beaked nose, and owl-like eyes.
Is there a connection between Gottron syndrome and Ehlers Danlos?
Gottron syndrome is thought to be inherited as an autosomal recessive genetic trait. Only about 40 cases have been reported in the medical literature. There is some debate in the literature regarding a possible relationship between Gottron syndrome and Ehlers-Danlos syndrome, type IV. Some clinicians believe the terms are synonymous.