Both sexes share a common plan: gonads (testes or ovaries) that make gametes and sex steroids, a system of ducts that transports the gametes, accessory glands that add secretions, and external genitalia. Male and female organs develop from the same indifferent primordia, so every structure has a homologue in the other sex — testis and ovary, scrotum and labia majora, penis and clitoris, corpus spongiosum and bulbs of the vestibule, bulbourethral and greater vestibular glands, prostate and paraurethral glands. Recognising these homologies makes the anatomy and its developmental anomalies much easier to learn.
In the male, the paired testes in the scrotum produce spermatozoa continuously from puberty in the seminiferous tubules and secrete testosterone from interstitial Leydig cells. Sperm pass through the epididymis (where they mature and are stored), the ductus deferens, the ejaculatory duct and the urethra, which runs through the prostate, the external urethral sphincter and the corpus spongiosum of the penis. The seminal vesicles, prostate and bulbourethral glands contribute most of the volume of semen. Erection, emission and ejaculation are coordinated by the parasympathetic, sympathetic and somatic (pudendal) nervous systems respectively.
In the female, the ovaries in the lateral pelvis contain a finite pool of oocytes established before birth. Each month a cohort of follicles grows and usually one releases a secondary oocyte at ovulation. The fimbriated uterine tube captures it, and fertilisation normally occurs in the ampulla. The early embryo travels to the uterus over 3–4 days and implants in the hormonally prepared endometrium. The cervix guards the uterine cavity, and the vagina forms the birth canal and receives the penis during intercourse. The mammary glands are accessory reproductive organs that nourish the newborn.
Reproduction is orchestrated by the hypothalamic–pituitary–gonadal (HPG) axis: pulsatile GnRH drives pituitary LH and FSH, which stimulate gametogenesis and sex steroid production; sex steroids and inhibin feed back on the hypothalamus and pituitary. In men this produces a steady, tonic state. In women the interplay of feedback produces the ovarian cycle (follicular phase → ovulation → luteal phase) and the parallel uterine (menstrual) cycle (menstrual → proliferative → secretory phase), including the unique switch to positive feedback that generates the mid-cycle LH surge.
The reproductive life cycle runs from sex determination in the embryo (SRY on the Y chromosome directs testis formation), through a quiescent childhood, puberty (reactivation of the GnRH pulse generator), the reproductive years, and — in women — menopause when the follicle pool is exhausted (median ≈51 years). Pregnancy reshapes maternal physiology: the placenta becomes the fetal lung, gut, kidney and a major endocrine organ, and the cardiovascular, respiratory, renal and metabolic systems all adapt. Clinically, the system accounts for common emergencies (ectopic pregnancy, testicular torsion), common cancers (breast, prostate, cervix, ovary, testis) and the large burden of infertility and sexually transmitted infection.
Development
Genetic sex is fixed at fertilisation, but the gonads and ducts are initially indifferent. Primordial germ cells arise from the epiblast, appear in the yolk-sac wall near the allantois in week 4 and migrate along the dorsal mesentery to the gonadal (genital) ridges by week 6. Both sexes possess two duct pairs: the mesonephric (Wolffian) and paramesonephric (Müllerian) ducts.
In a 46,XY embryo, SRY on the Y chromosome (week 6–7) up-regulates SOX9, turning supporting cells into Sertoli cells, which form testis cords and secrete anti-Müllerian hormone — the Müllerian ducts regress. Leydig cells, stimulated by placental hCG, secrete testosterone, which stabilises the Wolffian ducts into the epididymis, ductus deferens, seminal vesicle and ejaculatory duct; DHT (5α-reductase) masculinises the external genitalia (genital tubercle → glans and body of penis; urethral folds → spongy urethra; labioscrotal swellings → scrotum) and the prostate (urogenital sinus). The testes descend guided by the gubernaculum: a transabdominal phase (≈10–15 weeks, INSL3-dependent) and an inguinoscrotal phase (≈25–35 weeks, androgen-dependent), preceded by an outpouching of peritoneum, the processus vaginalis, which normally closes around birth.
In a 46,XX embryo, without SRY (and with WNT4/RSPO1/FOXL2 signalling) the gonad becomes an ovary; without AMH the Müllerian ducts persist — their cranial unfused parts form the uterine tubes and their caudal fused parts form the uterovaginal primordium (uterus, cervix, upper vagina); the lower vagina comes from the sinovaginal bulbs of the urogenital sinus. Without testosterone the Wolffian ducts regress (remnants: epoophoron, paroophoron, Gartner duct cysts). The genital tubercle forms the clitoris, urethral folds the labia minora and labioscrotal swellings the labia majora; the gubernaculum becomes the ovarian and round ligaments.
Anomalies follow logically: hypospadias (incomplete fusion of the urethral folds; ventral meatus), cryptorchidism, patent processus vaginalis (indirect inguinal hernia, hydrocele), Müllerian fusion defects (bicornuate, septate, didelphys uterus), Müllerian agenesis (MRKH syndrome), and differences of sex development such as congenital adrenal hyperplasia and androgen insensitivity.