Congenital hypothyroidism (CH) is a relatively frequent congenital endocrine disorder, caused by defective production of thyroid hormones (THs) at birth. Because THs are essential for the development of normal neuronal networks, CH is also a common preventable cause of irreversible intellectual disability (ID) in children. Prolonged hypothyroidism, particularly during the THs-dependent processes of brain development in the first years of life, due to delays in diagnosis, inadequate timing and dosing of levothyroxine (l-thyroxine or l-T), the non-compliance of families, incorrect follow-up and the interference of foods, drugs and medications affecting the absorption of l-T, may be responsible for more severe ID. In this review we evaluate the main factors influencing levels of THs and the absorption of l-T in order to provide a practical guide, based on the existing literature, to allow optimal follow-up for these patients.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9218053PMC
http://dx.doi.org/10.3389/fendo.2022.859487DOI Listing

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