Scleroderma – Symptoms of Schmidmann’s Syndrome

The condition of Schmidmann’s syndrome is characterized by muscular atrophy. It’s the result of a disorder that results in the death of muscle fibers and the surrounding tissue. This leads to an unusual deformation of the spinal cord and neurological system. The result is that a child with Scleroderma may appear to be in perfect health, but in fact is severely limited physically.

The cause of Scleroderma can be many. Some theories suggest that genetic problems, such as cystic fibrosis, can result in a person developing Scleroderma. Environmental factors, such as exposure to toxins, lead to the development of the condition. Scleroderma can also be a result of poor nutrition, or it can even be caused by the medications used for treating other illnesses, such as asthma and diabetes.

Because Scleroderma can have such a wide range of causes, it’s important that anyone who thinks their child might have the syndrome consult a physician to learn more about the disorder. It is possible to live with Scleroderma, but the disease can cause significant disability. It’s also possible to overcome the limitations that come along with Scleroderma.

Symptoms of Scleroderma are very different in children than they are in adults. Because of this, treatment for the condition can vary depending on what form it’s in. Treatment can also vary depending on which organ the Scleroderma is affecting. Generally, though, any part of the body can be affected by Scleroderma.

A trip to the doctor is always the first step when symptoms of Scleroderma are suspected. A physical exam will help to determine whether or not the patient has Scleroderma. The doctor may also order special tests to confirm whether the Scleroderma is indeed Scleroderma. These tests include X-rays, CT scans, blood tests and an ultrasound. All of these tests will help determine if there is truly a problem with one or more parts of the body.

When evaluating the condition of patients, doctors use a checklist to determine if Scleroderma is present. These include such factors as skin lumps, unusual weight loss, inability to walk and loss of appetite. If a child exhibits these symptoms, they should be seen by a pediatrician as soon as possible. Though rare, other symptoms of Scleroderma can manifest in children as well, so it’s important that children and their parents are aware of the condition’s existence.

Since there is no cure for Scleroderma, treatment options will vary depending on what kind of Scleroderma the patient has. The doctor treating the patient will determine which treatment will best treat the symptoms of Scleroderma. In general, however, medicines such as steroids, anti-inflammatory drugs and surgery are used to treat Scleroderma.

Because there is currently no known treatment for Scleroderma, it is important that children who exhibit the syndrome be treated as soon as possible. Though rare, other diseases that affect the lungs can cause similar symptoms, so it is important that young patients are routinely screened for lung disease as well as Scleroderma. Though this disease affects only one percent of the population, it is not something to be taken lightly. If you have a child who displays any of these symptoms, be sure to contact a doctor as soon as possible. While Scleroderma is not a common condition, it does happen, and it can be life threatening for your child.

Children may show a few symptoms of Scleroderma. They may have breathing problems or feel like they are constantly cold. They may also seem to sweat a lot. Another way to tell if your child has Scleroderma is by noticing if they are unusually thin. Other symptoms of Scleroderma include skin that are scaly and patchy, weak teeth, weak bones and poor muscle tone. A child with Scleroderma may also be unable to sit up straight or walk without difficulty.

There are some risk factors associated with Scleroderma. Younger children are more likely to suffer from Scleroderma because of their immune system’s lower resistance to infections. It may also be possible for children to suffer from Scleroderma if they have a family history of the condition. If a parent or sibling has been diagnosed with Scleroderma, then there is a greater chance that their children may also suffer from the condition.

Because Scleroderma can be serious, it is important that you find out all you can about it. If you or someone in your family has been diagnosed with Scleroderma syndrome, you should learn as much as you can about the condition and about treatment. If you are concerned that your child may have Scleroderma syndrome, you should see your doctor and talk to him or her about the symptoms and risks associated with the condition. Remember, though, that although the syndrome is serious, it is not contagious. Therefore, you don’t have to worry about catching the disease from someone else.

April 5, 2021 Pumper