ea0029p27 | Adrenal cortex | ICEECE2012
Rubio-Almanza M.
, Navas-de Solis S.
, Tenes-Rodrigo S.
, Querol Ripoll R.
, Perez-Lazaro A.
, del Olmo-Garcia M.
, Merino-Torres J.
The Nonclassical Congenital Adrenal Hyperplasia (NCCAH) is an autosomal recessive disorder. The importance of the diagnosis in fertile women relies in its therapeutic implications, genetic counseling and antenatal care during pregnancy. Diagnosis is established by the presence of basal 17-OH-progesterone (17-OHP) levels ≧6 ng/ml or stimulated after ACTH test ≧15 ng/ml. Basal values between 2-6 ng/ml or stimulated between 1015 ng/ml would require further con...