| Obligatory | Must not donate |
| Additional Information | Glycogen storage disease (GSD) is the result of defects in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types. GSD in humans is genetic caused by an inborn error of metabolism (genetically defective enzymes) involved in these processes. Donation may present a risk to the donor, even for milder forms of glycogen storage disease |
| Reason for Change | This is a new entry |
This entry was last updated in
TDSG-BM Edition 203, Release 29