What is hypothyroidism?
What causes hypothyroidism?
What are the symptoms of hypothyroidism?
The symptoms of hypothyroidism may resemble other conditions or medical problems. Always consult your child's physician for a diagnosis.
How is hypothyroidism diagnosed?
|Congenital (present at birth) hypothyroidism is usually detected during the routine newborn screening. Blood samples taken will reveal abnormal levels of T4 (a hormone of the thyroid that regulates metabolism) and thyroid-stimulating hormone, or TSH (a hormone that helps to increase the size, number, and activity of the thyroid cells; stimulates the release of hormones that affect a person's metabolism and that are essential for normal growth and development), that may indicate thyroid problems. Further diagnosis may include a scan of the thyroid gland to check for abnormalities.|
Treatment of hypothyroidism:
|Specific treatment for hypothyroidism will be determined by your child's physician based on:|
Left untreated in newborns, hypothyroidism can lead to mental retardation. Untreated hypothyroidism may also lead to anemia, low body temperature, and heart failure. The goal of treatment is to restore the thyroid gland to normal function, producing normal levels of thyroid hormones.
Treatment may include prescription of thyroid hormones to replace the deficient hormones. Some children will require hormone replacement therapy for the rest of their lives, while others appear to outgrow the disorder, often by the age of 3. Regular monitoring of the child's thyroid hormone levels during the course of treatment, including a 30-day discontinuation of treatment to see how the thyroid responds, can help your child's physician diagnose your child's condition more accurately.
What is congenital hypothyroidism?
|Congenital hypothyroidism (CH) means the disorder is present at birth. CH is one of the most common, preventable causes of mental retardation. Children in the US are tested for the disorder during their standard newborn screening. Newborn screening is performed in newborns in state public health programs to detect certain genetic diseases for which early diagnosis and treatment are available. Approximately 1,400 infants per 5,000,000 newborns are diagnosed with CH shortly after birth each year. |
In about 10 percent of cases, congenital hypothyroidism is inherited by an autosomal recessive gene, which means that two copies of the gene are necessary to produce the condition and both males and females are equally affected.
Most children born with CH appear normal at birth, possibly because the maternal thyroid hormones have sustained the infant's normal thyroid function in the womb. However, a significant sign that the infant may have hypothyroidism are low T4 (thyroxine, a hormone secreted by the thyroid gland which regulates metabolism) levels and high TSH (thyroid-stimulating hormone, a hormone that helps to increase the size, number, and activity of the thyroid cells; stimulates the release of hormones that affect a person's metabolism and that are essential for normal growth and development) levels (greater than 40 mU/L). However, researchers have found that some infants with CH will have low T4 levels, but normal TSH levels.
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