(M34.8) Other forms of systemic sclerosis

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589 161 in individuals diagnosis other forms of systemic sclerosis confirmed
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30 703 deaths with diagnosis other forms of systemic sclerosis
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5% mortality rate associated with the disease other forms of systemic sclerosis

Diagnosis other forms of systemic sclerosis is diagnosed Women are 60.53% more likely than Men

116 268

Men receive the diagnosis other forms of systemic sclerosis

8 382 (7.2 %)

Died from this diagnosis.

100
95
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55
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472 893

Women receive the diagnosis other forms of systemic sclerosis

22 321 (4.7 %)

Died from this diagnosis.

Risk Group for the Disease other forms of systemic sclerosis - Men aged 50-54 and Women aged 55-59

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In Men diagnosis is most often set at age 5-89
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Less common in men the disease occurs at Age 0-5, 90-95+Less common in women the disease occurs at Age 0-1, 90-95+
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In Women diagnosis is most often set at age 0-89

Disease Features other forms of systemic sclerosis

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Absence or low individual and public risk
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Other forms of systemic sclerosis - what does this mean

Other forms of systemic sclerosis (also known as scleroderma) are a group of autoimmune diseases characterized by an overproduction of collagen in the skin and other organs, leading to hardening and thickening of the skin, as well as inflammation and damage to other organs. these other forms of systemic sclerosis can be caused by a combination of genetic and environmental factors, such as exposure to certain toxins or viruses.

What happens during the disease - other forms of systemic sclerosis

Other forms of systemic sclerosis are caused by an abnormal immune response, where the body's immune system mistakenly attacks healthy tissue. this can cause inflammation and damage to the blood vessels, skin, and other organs. in some cases, this immune response can lead to the formation of scar tissue, which can cause further damage to the organs.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Complete physical examination
  • Laboratory tests including complete blood count, erythrocyte sedimentation rate, and C-reactive protein
  • Urinalysis
  • X-rays of the chest and abdomen
  • CT or MRI scans of the chest and abdomen
  • Skin biopsy
  • Pulmonary function tests
  • Echocardiogram
  • Electrocardiogram
  • Ultrasonography of the abdomen
  • Capillaroscopy

Treatment and Medical Assistance

Main goal: To reduce symptoms and improve quality of life.
  • Medication to reduce inflammation and prevent organ damage
  • Physical therapy to improve joint movement and reduce pain
  • Occupational therapy to help with daily activities
  • Counseling to manage stress and emotional issues
  • Nutritional counseling to improve diet and nutrition
  • Pulmonary rehabilitation to improve breathing and lung function
  • Alternative therapies such as acupuncture, meditation, and yoga
  • Surgery to correct deformities or repair damaged organs
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13 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Other forms of systemic sclerosis - Prevention

The best way to prevent other forms of systemic sclerosis is to avoid environmental triggers such as extreme temperatures, smoking, certain medications, and infections. additionally, it is important to practice healthy lifestyle habits, such as eating a balanced diet, getting regular exercise, and managing stress. additionally, it is important to seek treatment for any underlying conditions that could be contributing to the development of systemic sclerosis.