A young boy with ventricular arrhythmias and thyroid dysgenesis: two genes are not enough?
Abstract Congenital hypothyroidism (CH) may be caused by biallelic variants in the TSHR gene. CH due to thyroid dysgenesis has also been linked to pathogenic variants of the nucleotide kinase 2, homeobox 5 (NKX2-5) gene, which can also cause sudden cardiac death from ventricular arrhythmia. In parti...
Furkejuvvon:
| Váldodahkkit: | , , , , , , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Sociedade Brasileira de Endocrinologia e Metabologia
2023-01-01
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| Ráidu: | Archives of Endocrinology and Metabolism |
| Liŋkkat: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972023000100143&tlng=en |
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