Diagnostic Testing Service

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