At this time, there is no known cure for Hereditary pediatric Behcet-like disease. However, there are medications that can be used to manage the symptoms of the disease. These medications include non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, immunosuppressants, and biologic agents. Additionally, lifestyle modifications such as avoiding triggers, stress management, and physical therapy may help to reduce symptoms.

1. Family history of the disease
2. Genetic predisposition
3. Certain environmental factors, such as exposure to certain viruses or bacteria
4. Certain medications, such as antibiotics or immunosuppressants
5. Certain lifestyle factors, such as smoking or poor nutrition
6. Certain autoimmune diseases, such as lupus or rheumatoid arthritis

1. Non-steroidal anti-inflammatory drugs (NSAIDs): These medications can help reduce inflammation and pain.

2. Corticosteroids: These medications can help reduce inflammation and suppress the immune system.

3. Immunosuppressants: These medications can help reduce inflammation and suppress the immune system.

4. Biologic agents: These medications can help reduce inflammation and suppress the immune system.

5. Physical therapy: This can help reduce pain and improve mobility.

6. Surgery: In some cases, surgery may be necessary to treat complications of the disease.

7. Dietary changes: Eating a healthy diet can help reduce inflammation and improve overall health.

The exact cause of Hereditary pediatric Behcet-like disease is unknown. However, it is believed to be caused by a combination of genetic and environmental factors. It is thought that mutations in certain genes may be responsible for the development of the condition. Additionally, environmental triggers such as infections, stress, and certain medications may also play a role in the development of the disease.

The symptoms of Hereditary pediatric Behcet-like disease can vary from person to person, but may include:

- Recurrent oral ulcers
- Recurrent genital ulcers
- Skin rashes
- Eye inflammation
- Joint Pain and swelling
- Abdominal pain
- Neurological symptoms such as headaches, seizures, and confusion
- Anemia
- Enlarged lymph nodes
- Fever
- Fatigue

Hereditary pediatric Behcet-like disease is a rare, inherited disorder characterized by recurrent episodes of inflammation of the blood vessels (vasculitis) that can affect the skin, eyes, joints, and other organs. It is similar to Behcet's disease, but it is more severe and occurs in children. Symptoms may include fever, rash, joint pain, eye inflammation, and mouth sores. Treatment typically involves medications to reduce inflammation and suppress the immune system.