Glycogen storage disease - Bone Marrow and Peripheral Blood Stem Cell

Also known as: GSD

Essential information

Obligatory

Must not donate.

Supporting information

Additional information

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.

Version details:

BM-DSG Edition 203 Release 29 (24 April 2018)