Glycogen storage disease - Cord Blood

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. 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.

Version details:

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