Palavra-chave: CONGENITAL ADRENAL HYPERPLASIA

CHILDREN CYP3A7 GENE ANTHROPOMETRY DEFICIÊNCIA DA 21 HIDROXILASE DXA 17B-HYDROXYSTEROID DEHYDROGENASE TYPE 5 21-HYDROXYLASE DEFICIENCY HYPERTENSION TURNER SYNDROME METABOLIC SYNDROME BODY HEIGHT (MESH) FINAL HEIGHT ENDOCRINOLOGIA PEDIÁTRICA PRIMARY AMENORRHEA SRD5A2 GENE 11B-HYDROXILASE DEFICIENCY 17-HYDROXYLASE DEFICIENCY MUTAÇÕES EM CYP21 CYP21 GENE ADOLESCENTS BODY COMPOSITION PRENATAL TREATMENT CARDIOVASCUCULAR DYSFUNCTION POR GENE ALLELIC VARIANTS GENÉTICA GROWTH INSULIN RESISTANCE GENES CYP21A2 BONE MINERAL DENSITY HYPERGONADOTROPIC HYPOGONADISM LIPID PROFILE DEFICIÊNCIA DA ENZIMA 21-HIDROXILASE QUANTITATIVE ULTRASOUND OF PROXIMAL FALANGES TESTICULAR ADRENAL REST TUMOR FEMALE PSEUDOHERMAPHRODITISM C4 DEFICIENCY CYP21 MUTAÇÕES 21-DEOXICORTISOL EXTERNAL GENITALIA VIRILIZATION HSD17B5 GENE FEMINIZING GENITOPLASTY FETAL ANDROGEN SYNTHESIS PATHWAY BIOELECTRIC IMPEDANCE GENE CYP21A2 3B-HSD DEFICIENCY