Diagnostic
Testing Services
Gm1 gangliosidosis (GFB002)
Specimen type
EDTA whole blood
Contents
- GM1 Gangliosidosis is an inherited lysosomal storage disorder. Clinical signs of GM1 gangliosidosis include vision loss, difficulties in walking, loss of balance, head tremors, lethargy and weight loss.
- Koart, Siamese
