Palavra-chave: INTERSEX

17-HYDROXYLASE WT1 SOX3 QUIMERISM LEYDIG CELL DIAGNOSIS GONADS TURNER SYNDROME ADRENAL HYPOPLASIA DAX-1 OVOTESTIS MASS SPECTROMETRY HERMAPHRODITISM ANTI-MÜLLERIAN HORMONE SEX OF REARING ADRENAL HYPERPLASIA HYPOTHYROIDISM BLEPHAROPHIMOSIS PSEUDOHERMAPHRODITISM KARYOTYPE SEX DIFFERENTIATION ANDROGEN HYPOSPADIA ADRENAL HYPOGONADISM CHILD GROWTH TANDEM MASS SPECTROMETRY MUTATION INTERDISCIPLINARY INFERTILITY ANDROGEN INSENSIVITY PRECOCIOUS PUBERTY GONADOBLASTOMA DOWN SYNDROME ANDROGEN INSENSITIVITY SEX DIMORPHISM ADOLESCENT FRAISER SYNDROME INHIBIN B PRENATAL DIAGNOSIS SRY DIABETES MELLITUS NR0B1 SERTOLI CLITORIS DHX37 GENITOPLASTY EXOME IMMUNOASSAY TESTES GENE RECEPTOR NEONATAL 5 ALPHA REDUCTASE TESTOSTERONE ULTRASOUND PUBERTY HISTOLOGY 21-HYDROXYLASE 46,XY SERTOLI CELL LEYDIG LABORATORY SF-1 TREATMENT MÜLLERIAN DUCT XX MALE GONADAL DYSGENESIS NR5A1 SMALL GESTATIONAL AGE AGONADISM