PEPCK 1 deficiency (medical condition): A rare inherited disorder where deficiency of an enzyme (phosphoenolpyruvate carboxykinase-1) prevents fats and proteins being turned into glucose which causes various problems. In type 1, the enzyme deficiency occurs in the liquid part of the cells.
See also:
PEPCK 1 deficiency:
»Introduction: PEPCK 1 deficiency
»Symptoms of PEPCK 1 deficiency
These medical condition or symptom topics may be relevant to medical information for PEPCK 1 deficiency:
PEPCK 1 deficiency is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that PEPCK 1 deficiency, or a subtype of PEPCK 1 deficiency,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
PEPCK 1 deficiency (medical condition): See PEPCK 1 deficiency (disease information).
»Introduction: PEPCK 1 deficiency
»Symptoms of PEPCK 1 deficiency
These medical disease topics may be related to PEPCK 1 deficiency:
Source - NIH
Search to find out more about PEPCK 1 deficiency:
|
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.
