Genetic defects in thyroid hormone synthesis.

Détails

ID Serval
serval:BIB_8502CBB1EEEA
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Genetic defects in thyroid hormone synthesis.
Périodique
Current opinion in pediatrics
Auteur⸱e⸱s
Gillam M.P., Kopp P.
ISSN
1040-8703 (Print)
ISSN-L
1040-8703
Statut éditorial
Publié
Date de publication
08/2001
Peer-reviewed
Oui
Volume
13
Numéro
4
Pages
364-372
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Review
Publication Status: ppublish
Résumé
Thyroid hormone synthesis requires a normally developed thyroid gland, a properly functioning hypothalamic-pituitary-thyroid axis, and sufficient iodine intake. This article focuses on genetic defects in this axis. Defects that are primarily of developmental origin are discussed in our associated article in this issue. Defects in hormone synthesis usually are associated with the development of a goiter, provided that the bioactivity and action of thyrotropin (TSH) are not impaired. In contrast, hypoplasia of the gland may be caused by developmental defects, bioinactive TSH, or resistance to TSH at the level of the receptor or its signaling pathway. At the other end of the spectrum, hyperthyroidism may result from gain of function mutations in genes regulating growth and function.
Mots-clé
Congenital Hypothyroidism, Humans, Hyperthyroidism/congenital, Hyperthyroidism/genetics, Hypothyroidism/genetics, Thyroid Hormones/biosynthesis, Thyroid Hormones/genetics
Pubmed
Web of science
Création de la notice
30/12/2020 15:59
Dernière modification de la notice
31/12/2020 7:26
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