Palavra-chave: 21-HYDROXYLASE DEFICIENCY

CONGENITAL ADRENAL HYPERPLASIA HIPERPLASIA CONGÊNITA DAS SUPRA-RENAIS BODY HEIGHT (MESH) FETAL ANDROGEN SYNTHESIS PATHWAY SÍNDROME DE TURNER SRD5A2 GENE CYP21 GENE ANDROGEN INSENSIVITY HSD17B5 GENE CARDIOVASCUCULAR DYSFUNCTION 17B-HYDROXYSTEROID DEHYDROGENASE TYPE 5 NEONATAL SCREENING 17-HYDROXYPROGESTERONE 21-DEOXICORTISOL COMBINED ENZYMATIC DEFICIENCIES BONE MINERAL DENSITY 11B-HYDROXILASE DEFICIENCY PSEUDOHERMAPHRODITISM SEX AMBIGUITY FEMALE PSEUDOHERMAPHRODITISM FINAL HEIGHT GROWTH POR GENE EXTERNAL GENITALIA VIRILIZATION GENE CYP21A2 CYP3A7 GENE HERMAPHRODITISM ENDOCRINOLOGIA PEDIÁTRICA ALLELIC VARIANTS GENÉTICA GENES CYP21A2 TURNER SYNDROME ADRENAL HYPERPLASIA, CONGENITAL (MESH)