Applying this method, during the study period 126 patients were diagnosed with congenital steroid metabolism defects, including 106 patients with 21-hydroxylase deficiency, 5 patients with 11β-hydroxylase deficiency, one patient with 3β-hydroxysteroid dehydrogenase type II deficiency and 14 patients with 5α-reductase type 2 deficiency.
Ứng dụng kỹ thuật trong thời gian nghiên cứu đã giúp chẩn đoán rối loạn tổng hợp steroid bẩm sinh, trong đó 106 bệnh nhân thiếu 21 - hydroxylase, 5 bệnh nhân thiếu 11 β-hydroxylase, 1 bệnh nhân thiếu 3 β-hydroxysteroid dehydrogenase II, 14 bệnh nhân thiếu 5 α-reductase type 2.