hrp0082lbp-d3-1009 | (1) | ESPE2014
de Paula Michelatto Debora
, Grimaldi Larissa Magalhaes
, Alpiste Marcel Costa
, Baptista Maria Tereza Matias
, Guerra-Junior Gil
, Valente de Lemos-Marini Sofia Helena
, Palandi de Mello Maricilda
Background: Congenital adrenal hyperplasia, one of the most frequent autosome recessive disorders, is caused by defects in steroidogenic enzymes involved in the cortisol biosynthesis. Approximately 95% of cases are caused by a deficiency of the 21-hydroxylase enzyme. Its deficiency leads to androgen excess, consequently, to virilization and rapid somatic growth with accelerated skeletal maturation. Mutations in CYP21A2 are responsible for different forms of 21-hydroxylase defi...