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Transient congenital hypothyroidism – too short to be transient

Congenital hypothyroidism (CH) occurs due to thyroid dysgenesis, thyroid ectopy, and dyshormonogenesis. A proportion of CH is transient which might be due to iodine deficiency/excess or maternal antibody-mediated. Certain forms of dyshormonogenetic defects may cause transient hypothyroidism. Here is...

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Autor principal: Subramaniam, K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706545/
https://www.ncbi.nlm.nih.gov/pubmed/34341225
http://dx.doi.org/10.4103/jpgm.JPGM_1308_20
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author Subramaniam, K
author_facet Subramaniam, K
author_sort Subramaniam, K
collection PubMed
description Congenital hypothyroidism (CH) occurs due to thyroid dysgenesis, thyroid ectopy, and dyshormonogenesis. A proportion of CH is transient which might be due to iodine deficiency/excess or maternal antibody-mediated. Certain forms of dyshormonogenetic defects may cause transient hypothyroidism. Here is a report of a neonate with overt clinical and biochemical hypothyroidism, who on evaluation was found to have dyshormonogenesis with a homozygous mutation in dual oxidase 2 (DUOX2) gene. During infancy, she became euthyroid. Severe in utero deficiency of thyroid hormone, very short duration of hypothyroidism and first-reported mutation of the DUOX2 gene in the Indian subcontinent were interesting features in this infant.
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spelling pubmed-87065452022-01-10 Transient congenital hypothyroidism – too short to be transient Subramaniam, K J Postgrad Med Case Report Congenital hypothyroidism (CH) occurs due to thyroid dysgenesis, thyroid ectopy, and dyshormonogenesis. A proportion of CH is transient which might be due to iodine deficiency/excess or maternal antibody-mediated. Certain forms of dyshormonogenetic defects may cause transient hypothyroidism. Here is a report of a neonate with overt clinical and biochemical hypothyroidism, who on evaluation was found to have dyshormonogenesis with a homozygous mutation in dual oxidase 2 (DUOX2) gene. During infancy, she became euthyroid. Severe in utero deficiency of thyroid hormone, very short duration of hypothyroidism and first-reported mutation of the DUOX2 gene in the Indian subcontinent were interesting features in this infant. Wolters Kluwer - Medknow 2021 2021-07-08 /pmc/articles/PMC8706545/ /pubmed/34341225 http://dx.doi.org/10.4103/jpgm.JPGM_1308_20 Text en Copyright: © 2021 Journal of Postgraduate Medicine https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Subramaniam, K
Transient congenital hypothyroidism – too short to be transient
title Transient congenital hypothyroidism – too short to be transient
title_full Transient congenital hypothyroidism – too short to be transient
title_fullStr Transient congenital hypothyroidism – too short to be transient
title_full_unstemmed Transient congenital hypothyroidism – too short to be transient
title_short Transient congenital hypothyroidism – too short to be transient
title_sort transient congenital hypothyroidism – too short to be transient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706545/
https://www.ncbi.nlm.nih.gov/pubmed/34341225
http://dx.doi.org/10.4103/jpgm.JPGM_1308_20
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