Examples of using Systemic scleroderma in English and their translations into Hindi
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Ecclesiastic
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Other organs with systemic scleroderma.
Systemic scleroderma is usually seen in women ages 30 to 50.
Life expectancy of patients with systemic scleroderma.
Sometimes, with systemic scleroderma, trigeminal neuralgia.
Currently, lung damage servesthe main cause of death in systemic scleroderma.
In many patients with systemic scleroderma develops reflux esophagitis.
If the patient has all of these symptoms, then there is a suspicion of systemic scleroderma.
In some patients, systemic scleroderma develops cystic pneumatosis of the intestine;
The kidneys. Before the advent of modern methods of treating renal failure, it was the main cause of death in systemic scleroderma.
With systemic scleroderma it is possible development of the syndrome of impaired absorption.
The development of pulmonary hypertension in systemic scleroderma is usually accompanied by changes in the ECG.
Extension and atony of the lower parts of the esophagus andreflux esophagitis usually occur in advanced stages of systemic scleroderma.
With both forms of systemic scleroderma strongerthe skin of the distal parts of the extremities thickens.
In patients with mild or moderate arterial hypertension and insignificant proteinuria, renal dysfunction progresses less rapidly,and renal insufficiency develops only in the late stages of systemic scleroderma.
Symptoms of systemic scleroderma are changes in the skin, joints, gastrointestinal tract, lungs, heart, kidneys.
The word scleroderma means'hard skin' and in localised scleroderma, fat, fascia, muscle and bone may also be affected butnot internal organs as in systemic scleroderma.
However, even with this form of systemic scleroderma, the severity of skin manifestations may increase with time.
Acrosclerotic form of systemic scleroderma progresses more slowly, capturing onlydistal parts of the limbs and face or only the fingers.
Hair follicles, sweat and sebaceous glands at systemic scleroderma atrophy, because of what the skin becomes dry and rough.
Most often they are found in the acrosclerotic form of systemic scleroderma, although in later periods they can also appear in a diffuse form.
Less than 10% of patients with acrosclerotic form of systemic scleroderma after years after the onset of the disease develops pulmonary hypertension in the absence of severe pneumosclerosis.
However, children are 90% more likely to have localised scleroderma than the systemic disease[2].
In one type of scleroderma, called systemic sclerosis, you can also get hardening of some of your internal organs.
Systemic diseases: These are diseases that affect a number of organs and tissues, or affect the body as a whole, they include scleroderma, lupus, amyloidosis.
Systemic diseases: These are diseases that affect a number of organs and tissues, or affect the body as a whole, they include scleroderma, lupus, amyloidosis.
Researchers say they have discovered a promising target for new drugs that mightbe able to reverse the fibrosis process in systemic sclerosis or scleroderma- a rare disease that cuts short the lives of many patients and for which there is no cure or effective treatment.