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Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene
Thyroid hormones are crucial for development of the central nervous system. Congenital hypothyroidism (CH) is the most common preventable disease resulting in mental retardation. A neonatal screening test (NST) can detect a mild form of CH that can be treated at an early age. Generally after 3 years...
Sparad:
| I publikationen: | Ann Pediatr Endocrinol Metab |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Korean Society of Pediatric Endocrinology
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7136507/ https://ncbi.nlm.nih.gov/pubmed/32252219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2020.25.1.57 |
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