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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer - Medknow
2021
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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. |
format | Online Article Text |
id | pubmed-8706545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT subramaniamk transientcongenitalhypothyroidismtooshorttobetransient |