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Neonatal hypothyroidism Health Article
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Definition
Neonatal hypothyroidism is decreased thyroid hormone production in a newborn. In very rare cases, no thyroid hormone is produced. If the baby was born with the condition, it is called congenital hypothyroidism. If it develops soon after birth, it is referred to as hypothyroidism acquired in the newborn period.
Alternative Names
Cretinism; Congenital hypothyroidism; Hypothyroidism - infants
Causes, incidence, and risk factors
Hypothyroidism in the newborn may be caused by:
Incomplete development of the thyroid is the most common defect and occurs in about 1 out of every 3,000 births. Girls are affected twice as often than boys.
Symptoms
Most affected infants have few or no symptoms, because they only have a mild decrease in thyroid hormone production. However, infants with severe hypothyroidism often have a distinctive appearance. Symptoms may include:
This appearance usually develops as the disease gets worse. The child may also have:
Signs and tests
A physical exam may reveal:
Blood tests will be done to check thyroid function. Other tests that may be done include:
Treatment
Early diagnosis is very important. Most of the effects of hypothyroidism are easily reversible. Replacement therapy with thyroxine is the standard treatment of hypothyroidism. Once medication starts, thyroid blood tests are regularly done to make sure levels are within a normal range.
Expectations (prognosis)
Very early diagnosis generally results in a good outcome. Newborns diagnosed and treated in the first month or so generally develop normal intelligence. Untreated, mild hypothyroidism can lead to severe mental retardation and growth retardation. Critical development of the nervous system takes place in the first few months after birth. Thyroid hormone deficiency may cause irreversible damage.
Complications
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