|Values are valid only on day of printing.|
Diagnosis of GM1 gangliosidosis, Morquio B disease, and galactosialidosis
Not available or suitable for carrier detection.
Beta-galactosidase enzyme is deficient in the following conditions: GM1 gangliosidosis, Morquio syndrome B, and galactosialidosis.
Careful review of clinical findings will help distinguish between GM1 gangliosidosis and Morquio syndrome Type B.
A diagnosis of galactosialidosis must be additionally demonstrated by a deficiency of neuraminidase (NEURF / Neuraminidase, Fibroblasts).
This test is not suitable for carrier detection.