The thyroid is a gland in the lower neck. It makes hormones that regulate growth, brain development, and metabolism. Hypothyroidism is a low or absent production of these hormones. Congenital means the conditions is present since birth.
If this condition is not treated it can cause damage to the brain. This can lead to intellectual disability and abnormal growth.
In most cases, the cause is unknown, but it is probably genetic. The most common known causes are abnormal development of the thyroid gland or a defect in producing thyroid hormone. About 15% of cases are inherited.
Babies may have a temporary shortage in their thyroid hormones, which is more common if born before 40 weeks.
Factors that may increase the chance of congenital hypothyroidism include:
Symptoms or signs take time to develop. The symptoms of congenital hypothyroidism may include the following:
At birth, most infants are screened for this condition. Blood tests will be able to identify thyroid levels. Images of the thyroid may also be taken with:
The outcome is best if the condition is caught early. It is important to start treatment before the brain and nervous system are fully developed. If treatment is given early, it could prevent damage. Left untreated, the condition can lead to poor mental development and delayed growth.
Medication will treat the hypothyroidism. The medication will replace the missing hormone.
Once medication starts, the levels of thyroid hormones are checked often. This will help to keep the values within normal range. If values are kept within a normal range, there are no side effects or complications.
American Thyroid Association
Genetics Home Reference
Thyroid Foundation of Canada
American Academy of Pediatrics, Rose SR, Section on Endocrinology and Committee on Genetics, et al. Update of newborn screening and therapy for congenital hypothyroidism. Pediatrics. 2006;117(6):2290-2303.
Bongers-Schokking JJ, Koot HM, et al. Influence of timing and dose of thyroid hormone replacement on the development in infants with congenital hypothyroidism. J Ped. 2000;136(3):292-297.
Castanet M, Polak M, Leger J. Familial forms of thyroid dysgenesis. Endocr Dev. 2007;10:15-28.
Gruters A, Krude H, Biebermann H. Molecular genetic defects in congenital hypothyroidism. Europ J Endocr. 2004;151 Suppl 3:U39-U44.
Congenital hypothyroidism. EBSCO DynaMed Plus website. Available at: http://www.dynamed.com/topics/dmp~AN~T116588/Congenital-hypothyroidism. Updated March 24, 2016. Accessed September 26, 2016.
LeFranchi SH, Austin J. How should we be treating children with congenital hypothyroidism. J Pediatr Endocrinol Metab. 2007;20(5):559-578.
Last reviewed March 2016 by Kim A. Carmichael, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.