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Scleroderma is an ongoing (chronic) disease that causes abnormal growth of connective tissue. It can affect the joints, skin, and internal organs. It is a rare degenerative disease and gets worse over time. There are 2 main types of scleroderma: localized and systemic. Localized scleroderma.
18 gru 2023 · Scleroderma is a condition in which skin symptoms arise from sclerosis, an autoimmune disease that sometimes affects internal organs. Look through pictures here.
When scleroderma does occur in children, the average age of onset of juvenile localized scleroderma (jLS) is approximately 6 to 8 years old, and the average age of onset in juvenile systemic sclerosis (jSSc) is 8 to 11 years old.
Parents and their children who have been diagnosed with scleroderma often seek out trusted resources regarding the disease and available treatments. On this page and the others linked to it, we do our best to share important information that can help you in your journey.
Pediatric Localized Scleroderma. Localized scleroderma is the more common form of scleroderma among children. Learn about what we know about the causes, who might get localized scleroderma, the different forms of the disease, diagnosis, treatment, and prognosis.
5 sie 2022 · Systemic scleroderma affects your child’s internal organs and could cause symptoms that include: Joint inflammation with stiffness and pain. Sores (ulcers), mostly on the fingertips. Digestive problems like heartburn, trouble swallowing, diarrhea, stomach cramps.
Scleroderma is a rare disease that has two main forms: localized scleroderma (LS) and systemic sclerosis (SSc). Both are chronic diseases, can present in different patterns (subtypes), and are associated with extracutaneous involvement in pediatric patients.
