What Are The Types of Juvenile Rheumatoid Arthritis

Types of Juvenile Rheumatoid Arthritis

JIA is a type of joint inflammation in adolescents or children, usually affecting joints at age 16 or younger. It can cause various symptoms in a range of joints (often a number of joints or a few joints), and it can lead to symptoms throughout the body. The most common symptoms include painful, swollen, stiff, red, hot, and impaired joints.

The immune system of the young body directly attacks its own cells and tissues, leading to juvenile idiopathic arthritis. It is unknown why this occurs, but genetics and environmental factors may be responsible. You can check out The Effects of Juvenile Rheumatoid Arthritis in this article.

The symptom of arthritis is displaying limp in the morning because of a stiff knee. In addition, children with a common affliction called systemic JRA present fever and a skin rash. These symptoms may fade quickly.

Types of Juvenile Rheumatoid Arthritis

  1. Pauciarticular
  2. Polyarticular
  3. Systemic

Pauciarticular JRA

 Pauciaticular JRA is a combination of about 50 percent of children with this chronic ailment, with fewer than three or four joints being affected. Prominent areas like the knee, ankle, and elbow are the most often affected. Although this condition is most often found in infants and young children, it rarely affects teenagers.

Pure Juvenile Rheumatoid Arthritis doesn’t have yet a known cause. But like other forms of rheumatoid arthritis, rheumatoid arthritis is an autoimmune disease that can happen when your body causes your immune system to attack your healthy and undamaged tissues.

Some children may have symptoms on a daily basis, while others can experience symptoms only during periods or flare-ups of their PJRA. Symptoms include swollen knee, shoulder, elbow, ankle, or other joints painful and stiff in the morning or after taking a nap; warm, red, or discolored joints that are hard to move.

Polyarticular RJA

Previously known as polyarticular juvenile idiopathic arthritis (formerly so-called polyarticular-onset juvenile rheumatoid arthritis [RA]), a subset of juvenile idiopathic arthritis (JIA) is known as polyarticular juvenile idiopathic arthritis (formerly polyarticular-onset juvenile rheumatoid arthritis ) when four joints are affected in the first six months of illness.

Red blood cells may be low, and enlarged organs and increased lymph nodes are indications of polyarticular juvenile idiopathic arthritis. Damage to joints or linings of the heart or lungs prompts inflammation.

Pharmaceutical agents that are used for the treatment of JAE have shown many different mechanisms of action, some of which remain mysterious. During initial treatment, the first line usually involves nonbiologic disease-modifying antirheumatic drugs (DMARDs), such as methotrexate.

Systemic RJA

Systemic onset juvenile rheumatoid arthritis has the distinction of being a rare form of systemic-onset juvenile idiopathic arthritis. The phrase “systemic” indicates that the condition often exerts its influence on the entire body. Symptoms can include fever, rash, and joint swelling. Often onset is between the ages of 5 and 10 years, and both boys and girls can be affected.

Fever, in a child with a high, periodic fever, is often a sign of sJIA. A rash may also develop on your skin. A joint pain symptom can occur, too.

Effectively treating systemic juvenile idiopathic arthritis with high dosages of glucocorticoids was attempted in order to approach disease control. However, in some instances, this condition could not be managed after heavy use of glucocorticoids.
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