There is no known cure for Peeling Skin Syndrome Type C. Treatment is focused on managing the symptoms and preventing infection. This may include the use of topical antibiotics, antifungal medications, and moisturizers. In some cases, systemic medications such as corticosteroids may be used to reduce inflammation.

1. Genetic predisposition: Peeling skin syndrome type C is caused by a genetic mutation in the TGM5 gene.

2. Age: Peeling skin syndrome type C is more common in children and young adults.

3. Exposure to environmental triggers: Exposure to certain environmental triggers, such as heat, cold, friction, and humidity, can cause the skin to peel.

4. Stress: Stress can cause the skin to peel in people with Peeling skin syndrome type C.

5. Certain medications: Certain medications, such as antibiotics, can cause the skin to peel in people with Peeling skin syndrome type C.

The treatments for Peeling Skin Syndrome Type C vary depending on the severity of the condition. Generally, treatments may include:

1. Topical medications such as corticosteroids, calcineurin inhibitors, and retinoids.

2. Oral medications such as antibiotics, antifungals, and antihistamines.

3. Phototherapy, which uses ultraviolet light to reduce inflammation and improve skin texture.

4. Surgery to remove affected skin.

5. Moisturizers and emollients to help keep the skin hydrated and reduce irritation.

6. Nutritional supplements to help improve skin health.

7. Stress management techniques to reduce the psychological impact of the condition.

The exact cause of Peeling Skin Syndrome Type C is unknown. However, it is believed to be caused by a genetic mutation that affects the production of certain proteins in the skin. This mutation is thought to be inherited in an autosomal recessive pattern, meaning that both parents must carry the mutated gene in order for a child to be affected.

The symptoms of Peeling skin Syndrome type C (PSSC) vary from person to person, but generally include:

-Skin peeling, especially on the hands and feet
-Dry, scaly skin
-Itching
-Redness
-Blisters
-Painful cracks in the skin
-Thickening of the skin
-Discoloration of the skin
-Scarring
-Hair loss
-Nail abnormalities
-Joint Stiffness and pain
-Eye Irritation and dryness

Peeling skin syndrome type C (PSSC) is a rare genetic disorder characterized by recurrent episodes of peeling of the skin, usually beginning in infancy. It is caused by mutations in the TGM5 gene, which is responsible for the production of an enzyme called transglutaminase 5. Symptoms of PSSC include recurrent episodes of peeling of the skin, usually beginning in infancy, and may include redness, itching, and blistering. In some cases, the skin may become thickened and scaly. Other symptoms may include nail abnormalities, hair loss, and eye problems. Treatment for PSSC is supportive and may include topical medications, moisturizers, and antibiotics.