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CREST syndrome is also known as systemic induration , morphea - linear , mixed connective disease , progressive systemic induration , limited dermatosclerosis and localized scleroderma .
CREST syndrome is a subtype ofscleroderma . The genuine significance of scleroderma is hardened peel .
CREST syndrome is a kind of autoimmune disorder . An autoimmune disorder is a condition in which the resistant arrangement of the body starts lash out and destruct its own salubrious tissue paper . CREST syndrome is a disorder of the connective tissue paper . CREST syndrome is a condition in which changes occur in the heftiness , internal organs , skin , and blood vessels of the consistency .
CREST syndrome commonly touch the peg and lower blazon , which are often link with the changes of the tegument . CREST syndrome may also feign the throat and face in few of the cases . CREST syndrome happen in the digestive piece of ground leads to serious lung and center disorders .
Treatment for CREST syndrome is very hard , as there is no proper cure available to process the condition . Therefore its treatment extremely focus on reducing the symptoms to prevent serious complication .
Types of CREST Syndrome or Systemic Sclerosis
CREST Syndrome or Systemic Sclerosis Is Broadly Classified Into Two Types
Epidemiology of CREST Syndrome or Systemic Sclerosis
The recorded proportion of male and female is found as 1:10,000 in females and 4:1 in male . CREST syndrome usually sham people between the eld chemical group of 25 to 55 old age , however the disease may strike at any age . CREST syndrome is very rare among child . female person are more prone to CREST syndrome when equate to males . cosmopolitan ratio of males and female in CREST syndrome is record as 1:4.6 . In United States women of African descent often get affected with CREST syndrome when compare to the womanhood of European origin . Choctaw Native Americans also cover higher rates of CREST syndrome than other races .
Causes and Risk Factors for CREST Syndrome or Systemic Sclerosis
The exact cause of CREST syndrome is unknown . CREST syndrome is suspected to be an autoimmune disorder . This happens when the body ’s immune organization starts producing autoimmune antibodies in ordering to attack its own healthy tissues . Individuals who often develop too much collagen in their skin and other organs tend to get impress with CREST syndrome . Generally CREST syndrome affects people in the years group of 25 to 55 years . CREST syndrome also may affect turgid regions of the hide and organs like lung , kidney and heart .
Signs and Symptoms of CREST Syndrome or Systemic Sclerosis
Although CREST syndrome affects the tegument , whole body may also get affected .
Treatment for CREST Syndrome or Systemic Sclerosis
There is no proper curative available for treat CREST syndrome . Therefore , its handling concentrates on control the symptoms so as to preclude complications .
Investigations for CREST Syndrome or Systemic Sclerosis
A complete immanent and strong-arm interrogation is perform to diagnose CREST syndrome . Hard , besotted , boneheaded skin is a common determination on physical examination .
Blood Tests May Include:
Other Tests May Include
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