Scleroderma is an ongoing (chronic) disease that causes abnormal growth of connective tissue. It can affect the joints, skin, cartilage, and internal organs. It is a rare degenerative disease and gets worse over time.

There are two main types of scleroderma:

• Localized scleroderma. There are two forms of this type:
  • Morphea. This type causes one or more hard, oval-shaped, or irregular patches on any part of the body. Patches are whitish or darkened and sometimes have a purple or red-colored ring.
  • Linear. Lines or streaks of thickened skin form over one or more areas of the body, such as an arm, leg, or the head. Joint symptoms may also occur, such as pain, stiffness and trouble moving joints.
• Systemic scleroderma. This more severe type can affect the whole body. This type is more common in adults and rarely occurs in children.

Scleroderma is thought to be an autoimmune disease. This means the symptoms are caused by the body attacking its own healthy tissues. Genes play a role in the disease, but it is not passed on from parents to children. Some environmental factors may also play a role.

Scleroderma can lead to scarring of the skin, joints, and internal organs. Symptoms can occur a bit differently in each child. They may include:

• Thick, swollen fingertips.
• Pale and tingly fingers that may turn numb when out in the cold or during emotional upset (Raynaud's phenomenon).
• Joint pain.
• Taut, shiny, darker skin on large areas, that may cause problems with movement.
• Spider veins.
• Calcium bumps on the fingers or other bony areas.
• Frozen (immobile) fingers, wrists, or elbows because of scarring, hardening and tightness of the skin.
• Sores on fingertips and knuckles.
• Grating noise as inflamed tissues move.
• Scarring of the esophagus, leading to heartburn and trouble swallowing.
• Scarring of the lungs, leading to shortness of breath.
• Heart failure and abnormal heart rhythms.
• Kidney disease.
• Fatigue and muscle weakness.

Symptoms of localized sclerosis may include:

• Shiny, thickened patches of skin.
• Lighter or darker (discolored) skin.
• Joint tightness.

These symptoms can seem like other health conditions. Make sure your child sees a doctor for a diagnosis.

Your child's doctor will ask about your child's health history and do a physical exam. Diagnosis is based on the changes in the skin and internal organs. An antibody test may help show the type of scleroderma. Your child may need other tests, such as:

• Blood and urine tests. These can help find any problems with blood counts, or kidney or liver function.
• Skin biopsy. A small piece of skin may be removed and sent for testing
• Electrocardiogram (ECG). This test records the heart's electrical activity, shows abnormal rhythms, and finds heart muscle damage. An ECG may be done to find changes in the heart muscle tissue due to scleroderma.
• Echocardiogram. This test uses sound waves to create a moving image of the heart and its valves. It looks at the structure and function of the heart.
• Pulmonary function test. This is a breathing test to make sure your child's lungs are working properly.
• X-ray. This test uses a small amount of radiation to create images of internal tissues, bones, and organs. X-rays may show changes in bone, soft tissues, and organs caused by scleroderma.

Treatment will depend on your child's symptoms, age, and general health. It will also depend on how severe the condition is.

There is no cure for scleroderma, but treatment can help manage symptoms. Some cases of morphea scleroderma may clear up on their own. Treatment may include:

• Medicine to ease pain. These include nonsteroidal anti-inflammatory drugs or corticosteroids.
• Medicine to slow the skin thickening process and delay damage to internal organs (penicillamine).
• Medicine to weaken the immune system (immunosuppressive medicines).
• Treatment of specific symptoms, such as heartburn and Raynaud's phenomenon.
• Physical therapy and exercise, to maintain muscle strength.
• Skin protection. Using sunscreen, applying moisturizers, using a humidifier, and avoiding irritants and cold exposure can all help manage the skin thickening process.
• In rare cases, orthopedic hand or cosmetic surgery to correct severe joint or skin deformities or scars.

Talk with your child's doctor about the risks, benefits, and possible side effects of all medicines.

Problems from scleroderma vary depending on the type of the disease and how severe it is. Treatment may prevent or reduce problems. Possible problems may include:

• Thickened, tight skin.
• Arthritis.
• Seizures.
• Behavior and learning problems.
• Vision changes.
• GERD (gastroesophageal reflux) or heartburn.
• Less lung function.
• Heart and kidney damage.

Work with your child's doctor. Together you can make a treatment plan. The plan can help your child be active as much as possible in school, and in social and physical activities. Make life as normal as possible for your child. Encourage exercise and physical therapy and find ways to make it fun.

You can also help your child find a support group to be around other children with scleroderma. Work with your child's school to make sure your child has help as needed. Your child may also qualify for special help under Section 504 of the Rehabilitation Act of 1973.

Tell the doctor if your child's symptoms get worse or there are new symptoms.

• Scleroderma causes abnormal growth of connective tissue. It can affect the joints, skin, and internal organs.
• Scleroderma can affect one area of the body or affect the whole body. It is less common in children for it to affect the whole body.
• Localized scleroderma may affect patches of the skin on the torso, arms, legs, or head.
• There is no known cure for scleroderma. Treatment is focused on relieving pain and slowing down further damage to the body.

Tips to help you get the most from a visit to your child's doctor:

• Know the reason for the visit and what you want to happen.
• Before your visit, write down questions you want answered.
• At the visit, write down the name of a new diagnosis, and any new medicines, treatments, or tests. Also write down any new directions your doctor gives you for your child.
• Know why a new medicine or treatment is prescribed and how it will help your child. Also know what the side effects are.
• Ask if your child's condition can be treated in other ways.
• Know why a test or procedure is recommended and what the results could mean.
• Know what to expect if your child does not take the medicine or have the test or procedure.
• If your child has a follow-up appointment, write down the date, time, and purpose for that visit.
• Know how you can contact your child's doctor after office hours. This is important if your child becomes ill and you have questions or need advice.