SPHINGOLIPIDOSIS PANEL 3

Sphingolipidoses are a class of lipid storage disorders relating to sphin- golipid 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 10.000, but substantially more in certain populations such as Ashkenazi Jews.

  • Test Type:
  • Pre-test Information:
    Clinical details must accompany sample.
  • Report Delivery:
    Sample Daily by 4 pm; Report 4 days
  • Components:
    0

Sample Report