Two novel mutations in the thyroid peroxidase gene with goitrous hypothyroidism.
Endocr J
; 52(5): 643-5, 2005 Oct.
Article
en En
| MEDLINE
| ID: mdl-16284446
We encountered a Japanese patient with goitrous hypothyroidism due to iodide organification defect in the thyroid gland. Sequence analysis identified two novel mutations (E378K in exon 8 and a heterozygous 10 base deletion of the intron 15-exon 16 boundary) in the thyroid peroxidase (TPO) gene. As individuals with goitrous hypothyroidism caused by TPO gene mutation develop thyroid cancer, regular and careful follow-up for such patients must be done.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Hipotiroidismo Congénito
/
Yoduro Peroxidasa
Tipo de estudio:
Prognostic_studies
Límite:
Adolescent
/
Child, preschool
/
Humans
/
Male
/
Newborn
Idioma:
En
Revista:
Endocr J
Asunto de la revista:
ENDOCRINOLOGIA
Año:
2005
Tipo del documento:
Article
País de afiliación:
Japón
Pais de publicación:
Japón