Palavra-chave: 21-HYDROXYLASE DEFICIENCY

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