Suitable for patients with various glucose metabolism issues, insulin resistance, and familial hyperinsulinism. However, it does not detect conditions caused by imprinting errors or uniparental disomy.
Incorporates genes linked to chronic pancreatitis and can also serve for differential diagnosis, as it encompasses genes associated with pancreatic cancer.
Designed for patients suspected of having Congenital Adrenal Hyperplasia (CAH), a group of inherited disorders affecting adrenal gland function and steroid hormone production. The analysis includes the CYP21A2 gene, which is deficient in over 90.0% of CAH cases.