Advances in genetic research of congenital hypothyroidism in China / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
;
(12): 243-250, 2018.
Article
Dans Chinois
| WPRIM
| ID: wpr-300356
ABSTRACT
Congenital hypothyroidism (CH), which results from insufficient thyroid hormone biosynthesis, is one of the most common neonatal endocrine disorders. Thyroid dysgenesis and thyroid dyshormonogenesis are the two causes of CH and either one will lead to deficiencies of enzymes during thyroid hormone biosynthesis and insufficient thyroid hormone biosynthesis. Recently, researchers have performed extensive studies on genetics of CH. This paper reviews genes reported to be associated with CH in China.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Thyroglobuline
/
Facteurs de transcription
/
Récepteur TSH
/
Hypothyroïdie congénitale
/
Facteur de transcription PAX-8
/
Génétique
/
Iodide peroxidase
/
Protéines membranaires
Limites du sujet:
Humains
langue:
Chinois
Texte intégral:
Chinese Journal of Contemporary Pediatrics
Année:
2018
Type:
Article
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