Progressive systemic sclerosis, also known as systemic scleroderma, is a rare autoimmune disease that primarily affects the skin and connective tissues throughout the body. This chronic condition is characterized by the abnormal production and accumulation of collagen, leading to thickening and hardening of the skin and other organs.
While the exact cause of progressive systemic sclerosis remains unknown, researchers believe that a combination of genetic, environmental, and immune system factors may contribute to its development. Although anyone can develop this condition, it predominantly affects women between the ages of 30 and 50.
Individuals with progressive systemic sclerosis often experience a variety of symptoms, which can vary in severity. Common symptoms include skin thickening, joint pain, muscle weakness, Raynaud's phenomenon (which causes color changes in the fingers and toes in response to cold or stress), and gastrointestinal problems.
Here are some key features of progressive systemic sclerosis:
Early diagnosis and management of progressive systemic sclerosis are crucial to prevent further complications and manage symptoms effectively. If you experience any of the symptoms associated with this condition, it is important to consult a healthcare professional for an accurate diagnosis and appropriate treatment plan.
Note: This article provides an overview of progressive systemic sclerosis and its key features. It is essential to consult a healthcare professional or specialist for accurate information about diagnosis, treatment, and management of this condition.
Progressive systemic sclerosis, also known as systemic sclerosis or scleroderma, is a rare chronic autoimmune disease that affects the connective tissues of the body. It is characterized by the hardening and tightening of the skin, as well as damage to internal organs such as the heart, lungs, and kidneys. While there is no known cu...
To see full information about treatment please Sign up or Log in