Transient congenital hypothyroidism due to heterozygous mutations of THOX2 (Q86205): Difference between revisions
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Defeitos no gene tireoide-oxidase 2 (THOX2) resultam na ausência de H2O2, essencial para a síntese dos hormônios tireoidianos. Entretanto, mutações heterozigóticas neste gene provocam hipotireoidismo congênito transitório. | |||
| description / en | description / en | ||
Defects in the thyroid oxidase 2 (THOX2) gene result in a lack of H2O2, which is a protein essential for thyroid hormone synthesis. Therefore, heterozygous mutations in this gene lead to transient congenital hypothyroidism. | |||
Revision as of 11:34, 15 August 2026
Defects in the thyroid oxidase 2 (THOX2) gene result in a lack of H2O2, which is a protein essential for thyroid hormone synthesis. Therefore, heterozygous mutations in this gene lead to transient congenital hypothyroidism.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1663592623 |
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| English | Transient congenital hypothyroidism due to heterozygous mutations of THOX2 |
Defects in the thyroid oxidase 2 (THOX2) gene result in a lack of H2O2, which is a protein essential for thyroid hormone synthesis. Therefore, heterozygous mutations in this gene lead to transient congenital hypothyroidism. |
