SPHINGOLIPIDOSIS PANEL 2
Sphingolipidoses are a class of lipid storage disorders relating to sphingolipid metabolism. They are generally inherited in an autosomal recessive fashion, but notably Fabry disease is X-linked recessive.Taken together, sphingolipidoses have an incidence of approximately 1 in 10000, but substantially more in certain populations such as Ashkenazi Jews.
Parameter(s) covered : 2
Report Frequency: Sample Daily by 4 pm; Report 4 days
Special Instruction: Give brief clinical history.
Price : ₹ 4400.00
Parameters
- Beta Glucocerebrosidase
- Sphingomyelinase