Thyroid Screening for Babies of Mothers with Thyroid Disease
Extra thyroid checks for babies when the mother has Graves' disease or Hashimoto's thyroiditis, on top of the routine newborn screen.
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- Author
- Dr Jubal John, FRACP
- Category
- medical guides
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Take-home
If you have Graves’ disease or Hashimoto’s thyroiditis, thyroid antibodies can cross the placenta and affect your baby’s thyroid for the first few weeks or months. Babies of mothers with these conditions need extra blood tests on top of the routine newborn screen. Any problems are usually temporary, respond well to treatment, and leave no long-term effects.
Who needs extra screening?
Every baby in Victoria has a newborn bloodspot screen (the heel-prick test) at 48–72 hours. This checks for congenital hypothyroidism and about 30 other conditions. It is an important screen, but it is not designed to pick up antibody-driven thyroid problems that develop in the first days or weeks of life.
Your baby needs additional thyroid checks if you:
- Have active or previously treated Graves’ disease (even if your thyroid was removed or ablated)
- Have Hashimoto’s thyroiditis with high TSH-receptor-blocking antibodies
- Took antithyroid medications (carbimazole, methimazole, propylthiouracil) during pregnancy
- Had high TRAb levels on testing in pregnancy
Why it matters
Mother’s thyroid antibodies travel across the placenta and can act on the baby’s thyroid for weeks to months, even if mum has been well controlled. There are two patterns:
Graves’ antibodies (TSH-receptor stimulating)
- Can cause neonatal hyperthyroidism (overactive thyroid)
- Typically appears within the first 2 weeks of life, occasionally later
- Affects around 1–5% of babies of mothers with Graves’ disease
Hashimoto’s antibodies (TSH-receptor blocking)
- Can cause transient hypothyroidism (underactive thyroid)
- Much less common
- Usually settles as antibodies clear
Your baby’s testing schedule
Typical plan (individualised to your baby)
- At birth (cord blood): TSH, Free T4, and TRAb if mother has Graves’ disease
- Day 3–5: repeat TSH and Free T4
- Day 10–14: TSH and Free T4, this is the critical window when hyperthyroidism often appears
- 4–6 weeks: final check as maternal antibodies decline
The routine newborn bloodspot test at 48–72 hours stays in place in addition to these.
Testing frequency increases if any result is abnormal or symptoms appear.
Signs to watch for at home
Neonatal hyperthyroidism (overactive thyroid)
Usually appears in the first 2 weeks.
- Irritability, agitated feeds, trouble settling
- Poor weight gain despite feeding well
- Fast heart rate (over 160 beats per minute at rest)
- Sweating or flushing
- Prominent or “starey” eyes
- An enlarged neck (goitre)
- Loose stools
Neonatal hypothyroidism (underactive thyroid)
- Prolonged jaundice beyond 2 weeks
- Very sleepy or hard to wake
- Poor feeding
- Constipation
- Cool, mottled skin
- Large tongue or poor muscle tone
- Hoarse cry
- Umbilical hernia
Contact your paediatrician today if you see these signs
Don’t wait for the next scheduled test. Early treatment prevents problems.
Treatment
For hyperthyroidism
- Antithyroid medications (methimazole or propylthiouracil)
- Beta-blockers if the heart rate is high
- Close monitoring: daily vitals in hospital and weekly blood tests
- Duration: usually 2–3 months while maternal antibodies clear
For hypothyroidism
- Thyroxine (levothyroxine): a tiny once-a-day tablet crushed into a little breast or formula milk
- Dose based on weight and blood levels
- Monitoring: thyroid function tested every 2–4 weeks initially, then less often
- Duration: often only until antibodies clear (3–6 months); permanent treatment is rare in this antibody-driven form
Long-term outlook
Antibody-driven thyroid problems clear as the maternal antibodies leave the baby’s system, usually by 3–6 months. With proper monitoring and treatment:
- Growth and development stay on track
- Babies do not have a higher risk of thyroid disease later in life
- Treatment can usually be stopped completely once antibodies clear
- Follow-up is with a paediatric endocrinologist initially, then gradually spaced out
When to seek help
Green — usually fine
All tests normal, baby well
- Continue scheduled follow-up
- Routine MCH visits
Amber — be alert
Ring your paediatrician today if:
- Your baby is more unsettled, sleepy, or poorly feeding than expected
- Feeds are taking much longer than usual
- You notice a lump in the neck or prominent eyes
- Jaundice is still visible after 2 weeks
Red — act now
Call 000 or go to the nearest emergency department now if:
- Your baby is very fast-breathing or working hard to breathe
- Heart rate feels very fast and baby looks distressed
- Your baby is floppy, unresponsive, or has a seizure
- You cannot wake your baby for a feed
What about the standard newborn screen?
The Victorian newborn bloodspot screening at 48–72 hours is a separate test. It reliably detects congenital hypothyroidism (where a baby is born with a small, missing, or poorly developed thyroid) and other rare conditions, but it is not designed to detect antibody-driven thyroid disease that shows up later. That is why your baby needs both sets of tests.
Summary
Key points to remember
- Babies of mothers with Graves’ or Hashimoto’s need extra thyroid tests
- Problems are usually temporary and respond quickly to treatment
- Watch for signs in the first 2–4 weeks and ring your paediatrician if you see any
- With follow-up, babies grow and develop normally
- Keep all scheduled appointments even if your baby seems fine



