CDGS5 (medical condition): A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1C has a ?1,3-glucosyl-transferase enzyme defect.
See also:
Congenital disorder of glycosylation type 1C:
»Introduction: Congenital disorder of glycosylation type 1C
»Symptoms of Congenital disorder of glycosylation type 1C
CDGS5: Another name for Congenital disorder of glycosylation type 1C (or close medical condition association).
»Introduction: Congenital disorder of glycosylation type 1C
»Symptoms of Congenital disorder of glycosylation type 1C
Some of the symptoms of CDGS5 incude:
See full list of 13 symptoms of CDGS5 (Congenital disorder of glycosylation type 1C)
These medical disease topics may be related to CDGS5:
Search to find out more about CDGS5:
|
What do you think about the features of this website? Take our user survey and have your say:
Tools & Services:
Medical Articles:
Search Specialists by State and City
By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.
Copyright © 2009 Health Grades Inc. All rights reserved.
