Pediatrics · MU Sofia

15. Physiology and phatology of puberty. Disturbances of calcium-phosphorous metabolism.Rickets

Covers the hormonal sequence of normal puberty in girls and boys, with a side-by-side table of their stages, then central and peripheral precocious puberty and the causes of delayed puberty. It moves on to calcium and phosphate control, with a hormone table, neonatal and childhood hypocalcaemia, and rickets: causes, signs, a nutritional versus X-linked comparison table, and treatment and prevention, ending with dental effects.

Inside: 6 sections · 4 tables · 16 flashcards · 5 min

Topic 15 of 30 in the MU Sofia syllabus for Pediatrics (Medicine, Year 5). The free AceMed note covers it in 6 sections, about 511 words (5 min of reading), with 16 flashcards.

In this note

  1. Introduction
  2. Normal puberty
  3. Precocious puberty
  4. Delayed puberty
  5. Calcium and phosphate control
  6. Rickets

Introduction

This topic joins two subjects: puberty, the change from child to adult body, and the control of calcium and phosphate, whose failure in a growing child causes rickets.

Normal puberty

The hypothalamus restarts pulsatile GnRH release (switched on by kisspeptin) → the pituitary releases LH and FSH → the gonads make oestradiol or testosterone and gametes. Separately, the adrenals make more androgens from about 6–8 years (adrenarche): pubic and axillary hair, body odour, acne.

Tanner stages 1 to 5 describe breast (girls), genitals (boys) and pubic hair. The orchidometer measures testicular volume.

Precocious puberty

Signs of puberty before 8 years in girls or 9 years in boys.

  • Tests: growth velocity, bone age (advanced), LH/FSH and sex steroids, GnRH stimulation test, pelvic ultrasound, MRI.
  • Treatment of central puberty: GnRH agonists (leuprorelin, triptorelin) to protect final height and for emotional reasons; treat the cause.

Delayed puberty

No breast development by 13 years in girls or testes under 4 mL by 14 years in boys (or no menarche by 15).

  • Constitutional delay (commonest, mostly boys; family history; delayed bone age; catches up).
  • Low gonadotrophins (hypogonadotropic): chronic illness, undernutrition, anorexia, intense sport, hypothyroidism, Kallmann syndrome (with loss of smell), pituitary tumours (craniopharyngioma).
  • High gonadotrophins (gonadal failure): Turner syndrome, Klinefelter syndrome, chemotherapy or radiotherapy.
  • Treatment: short courses of low-dose testosterone or oestrogen; treat the cause.

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