Add like
Add dislike
Add to saved papers

IMMUNE CHANGES IN NEWBORN INFANTS WITH GASTROINTESTINAL FAILURE REQUIRING INTENSIVE CARE.

Newborns in critical conditions, because of the natureof the immune system, have the greatest risk of realization of immune deficiency, especially with gastrointestinal failure. We analyzed 44 cases of diseases in newborns in critical conditions and 20 cases without and studied the clinical and laboratory signs of immunological disorders, organpathology, gene expressionToll-likereceptor type 2. In newborns requiring intensive care, the frequency of gastrointestinal failure registration in 40,9%. Gastrointestinal failure leads to increased amounts of other affected systems, severity of systemic inflammation, gene expressionToll-likereceptor type 2, a marker of apoptosis of lymphocytes-CD95+, inhibition lymphocyte germ of immune system due to fraction of CD4+,the severity of the clinical condition. In newbornsin intensive care gastrointestinal failure is recorded at a frequency of 40,9%, is a component of multiple organ dysfunction syndrome, increases the expression of the geneToll-likereceptor type 2, implements violation adequate response humoral immunity, activates apoptosis of lymphocytes, which increases the severity of the patients.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app