| Literature DB >> 34128397 |
Aryel Furman1, Zeina Hannoush1, Francisco Barrera Echegoyen1, Alexandra Dumitrescu2, Samuel Refetoff2,3,4, Roy E Weiss1.
Abstract
A family with congenital hypothyroidism was identified with two novel deleterious compound heterozygous thyroid peroxidase (TPO) mutations (c.962C>A, and c.1577C>T). Serum thyroid tests showed higher-than-expected serum-free thyroxine (T4) relative to TT3, while reverse triiodothyronine (rT3) was also elevated. Two siblings manifested a more severe phenotype of developmental delay compared with another sibling and were found to harbor an additional novel heterozygous deleterious iodothyronine deiodinase 1 (DIO1) mutation (c.395G>A). In the context of L-T4 replacement, the decreased D1 activity results in abnormal thyroid hormone metabolism with decreased triiodothyronine (T3) generation from L-T4 and may result in decreased T3 bioavailability during critical stages of development.Entities:
Keywords: congenital hypothyroidism; deiodinase; reverse T3; thyroperoxidase
Mesh:
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Year: 2021 PMID: 34128397 PMCID: PMC8917882 DOI: 10.1089/thy.2021.0210
Source DB: PubMed Journal: Thyroid ISSN: 1050-7256 Impact factor: 6.506