Palavra-chave: 21-HYDROXYLASE DEFICIENCY

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