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19001717 The Carrier Screening 18 test is a genetic test that screens for 18 specific genetic diseases.
1. Alpha Thalassemia
2. Beta Thalassemia
3. Galactose metabolism disorder
4. Phenylketonuria (PKU)
5. G6PD deficiency
6. Glycogen storage disease type 2 (Pompe disease)
7. Citrin deficiency
8. 5-alpha reductase deficiency
9. Copper metabolism disorder (Wilson disease)
10. Fabry disease
11. Non-syndromic hearing loss (GJB2)
12. Cystic Fibrosis
13. Usher syndrome (hearing impairment and vision loss)
14. Primary hyperoxaluria
15. Glucose metabolism disorder
16. Multiple acyl-CoA dehydrogenase deficiency (MADD)
17. Gaucher disease
18. Bloom syndrome
