Did You Know? Juvenile Dermatomyositis rarely occurs under age 2
JDM Begins in Children Under 16 and Affects 3-5,000 Children in the United States
Juvenile Dermatomyositis (JDM) is a rare autoimmune disease that most commonly occurs in children 5-10 years of age. It is an inflammatory condition that affects the muscles, skin and blood vessels. Dermatomyositis belongs to a group of diseases and disorders of the muscles called inflammatory myopathies. The cause is unknown; however, the leading theory is that the body’s immune system mistakenly directs inflammation against muscle cells and blood vessels in the skin and muscles, resulting in damage, rash and weakness.
01 | Common Signs and Symptoms
The two most common features of JDM are a violet-colored rash on the face, eyelids and on the areas around the nails, elbows, knees, chest and back; and progressive muscle weakness of the trunk of the body. This may affect the child’s ability to get out of a chair, off the floor or into a car.
Other symptoms include:
02 | Diagnosing JDM
In order to obtain a positive diagnosis of Juvenile Dermatomyositis, your Pediatric Rheumatologist will likely perform the following tests:
03 | JDM Treatment
Treatment can minimize inflammation, improve function and prevent disability. Remission is possible in many cases. Treatment options may include:
For additional resources on treatment options and finding support for JDM, please visit: http://www.myositis.org/learn-about-myositis/types-of-myositis/juvenile-dermatomyositis
References
https://www.cincinnatichildrens.org/health/j/jdms
https://www.rheumatology.org/I-Am-A/Patient-Caregiver/Diseases-Conditions/Dermatomyositis-Juvenile
http://www.arthritis.org/about-arthritis/types/juvenile-dermatomyositis-jd/