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.
Artigo
em Chinês
| 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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Tireoglobulina
/
Fatores de Transcrição
/
Receptores da Tireotropina
/
Hipotireoidismo Congênito
/
Fator de Transcrição PAX8
/
Genética
/
Iodeto Peroxidase
/
Proteínas de Membrana
Limite:
Humanos
Idioma:
Chinês
Revista:
Chinese Journal of Contemporary Pediatrics
Ano de publicação:
2018
Tipo de documento:
Artigo
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