Introduction
Thyroid hormone drives growth and brain development; adrenal hormones keep blood pressure, salt and sugar steady under stress. In children, missing these hormones harms the brain (thyroid) or can kill within days (adrenal crisis), so both are screened for or looked for actively.
Congenital hypothyroidism
About 1 in 2000–3000 births; the commonest preventable cause of intellectual disability. Causes: thyroid dysgenesis (absent, small or ectopic gland, about 85%), dyshormonogenesis (enzyme defects, often with goitre), central (pituitary), transient (maternal antibodies or drugs, iodine excess or lack).
- At birth most babies look normal (maternal T4 crosses the placenta), which is why newborn screening (TSH on the heel-prick sample) matters.
- Signs if missed: prolonged jaundice, poor feeding, constipation, sleepiness, hoarse cry, large tongue, umbilical hernia, dry skin, large posterior fontanelle, low tone; later delay and short stature.
- Treatment: levothyroxine 10–15 µg/kg a day, started within the first 2 weeks; children treated early have normal intelligence.
Acquired hypothyroidism
Usually autoimmune (Hashimoto) thyroiditis, girls, often with goitre, anti-TPO antibodies; more common in Down and Turner syndromes and type 1 diabetes. Clue in children: slowing growth with weight gain and delayed bone age; tiredness, constipation, cold intolerance, poor school work, delayed (or sometimes early) puberty. Treat with levothyroxine.