Obligatory | Must not dontate |
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. There is insufficient evidence to determine whether donations from a baby with a glycogen storage disease could present a risk to recipients. |
Reason for Change | This is a new entry |
This entry was last updated in
TDSG-CB Edition 203, Release 29