ey0016.13-7 | Endocrinology: Newborn Screening | ESPEYB16
L Gong
, X Gao
, N Yang
, J Zhao
, H Yang
, Y Kong
J Pediatr Endocrinol Metab 2019; 32(3): 253258. DOI: 10.1515/jpem-2018-0342• 44,360 neonates were screened for CAH as part of a pilot screening programme in Beijing.• In this prospective study, a CAH incidence of 1:7393 was found, and the most common 21 OHase mutation was c.293-13C/A>G.The authors describe the results of a ...