Congenital hypothyroidism

Below you will find more information about Congenital hypothyroidism from Medigest. If you believe that you are suffering from any of the symptoms of Congenital hypothyroidism it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Congenital hypothyroidism and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Congenital hypothyroidism comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Congenital hypothyroidism is also medically referred to as endemic cretinism which is characterized by the inadequate production of thyroid hormone among newborn infants. This typically occurs due to an anatomic defect in the infant's gland, which is categorized as an inborn defect of iodine deficiency or thyroid metabolism.


The diagnosis of congenital hypothyroidism is usually confirmed through the demonstration of the infant's elevated levels of TSH and the reduced levels of serum thyroid hormone. Some routinary laboratory testing can also be performed from time to time.


Treatments for congenital hypothyroidism value the importance of early diagnosis along with thyroid hormone replacement. It is best prevented through supplementation of iodine, which is usually found in salt. Other supplementary treatment include intramuscular injections of lipiodol or iodized oil in the body.

Symptoms and Signs

Among the prevalent signs and symptoms of congenital hypothyroidism include jaundice, hypotonia, hoarse cry, constipation, poor weight and stunted growth, abnormally large fontanelles, umbilical hernia, developmental delay, excessively dry and mottled skin and goiter.


Congenital hypothyroidism is primarily caused by the child's iodine deficiency, as well as the dysgenesis of the patient's thyroid gland, abnormalities in the TSH receptor, deiodinase defects, and pendred syndrome.

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