Palavra-chave: 21-HYDROXYLASE DEFICIENCY

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