Paediatrics: Congenital hypothyroidism
Hypothyroidism may be due to a number of conditions that result in the insufficient secretion of thyroid hormones.
Hypothyroidism may be due to a number of conditions that result in the insufficient secretion of thyroid hormones. Congenital hypothyroidism is a relatively common condition, occurring in approximately 1/4000 births. It is twice as common in girls as in boys.
The causes of congenital hypothyroidism include the following:
- Thyroid dysgenesis (85%): usually sporadic; resulting in thyroid aplasia/hypoplasia, ectopic thyroid (lingual/sublingual).
- Thyroid hormone biosynthetic defect (15%): hereditary, e.g. Pendred’ssyndrome.
- Iodine deficiency (rare UK; but common worldwide).
- Congenital TSH deficiency (rare): associated with other pituitary hormone deficiencies.
Usually non-specific; they are difficult to detect in the first month of life. They include:
- umbilical hernia;
- prolonged jaundice;
- hoarse cry;
- poor feeding;
- excessive sleepiness;
- dry skin;
- coarse faeces;
- delayed neurodevelopment.
In most developed countries there are national neonatal biochemical screening programmes.
- Test in 1st week of life.
- Blood spots—filter paper collection (e.g. ‘Guthrie card’).
- TSH (high) and/or fT4 (low) estimation.
Thyroid imaging is also recommended to determine whether the cause is due to thyroid dysgenesis or due to hormone biosynthetic disorder.
- Thyroid US.
Radionucleotide scanning (99Tc or 131I).
Without early hormone replacement therapy, a number of adverse sequelae may occur.
- Neurodevelopmental delay and mental retardation.
- Poor motor coordination.
- Poor growth and short stature.
The earlier the treatment with oral thyroid hormone replacement therapy is initiated the better the prognosis: levothyroxine (initial dose 10–15micrograms/kg/day).
Monitor serum TSH and T4 levels:
- Every 1–2mths 1st year; every 2–3mths age 1–2yrs; every 4–6mths age >2yrs.
- Maintain T4 level in the upper half of normal range; TSH in the lower end of the normal range.
Transient hyperthyro tropinaemia
This is uncommon and is usually detected at the time of neonatal thy-roid screening. It is characterized by slightly elevated serum TSH level in presence of otherwise normal serum T4 levels. It is probably due to the transplacental transmission of maternal thyroid antibodies to the child in utero. Presumed causes do not need treatment, but must be monitored. TSH levels that remain persistently elevated after a few months or low T4 levels should be treated with oral levothyroxine.