hrp0086p1-p38 | Adrenal P1 | ESPE2016
Miranda Mirela
, Carvalho Daniel
, Gomes Larissa
, Madureira Guiomar
, Marcondes Jose
, Billerbeck Ana Elisa
, Rodrigues Andressa
, Presti Paula
, Kuperman Hilton
, Damiani Durval
, Medonca Berenice
, Bachega Tania
Background: Most congenital adrenal hyperplasia (CAH) patients carry mutations derived from conversion events involving the pseudogene, and the remaining carry new mutations varying according to ethnicity. A good genotype-phenotype correlation is observed, allowing the use of molecular analysis in clinical practice.Objective and hypotheses: To review the molecular diagnosis in a large cohort of CAH patients in order to create a diagnostic panel in our po...