Mutation of thyroid peroxidase gene in 35 patients with congenital hypothyroidism.
- Author:
Hai-fei LI
1
;
Yi-xin LIU
;
Jian-sheng XIE
;
Bin CHEN
;
Su-li LI
Author Information
- Publication Type:Journal Article
- MeSH: Autoantigens; genetics; Case-Control Studies; Child; Child, Preschool; Congenital Hypothyroidism; genetics; DNA Mutational Analysis; Exons; Female; Humans; Infant; Iodide Peroxidase; genetics; Iron-Binding Proteins; genetics; Male; Mutation
- From: Chinese Journal of Pediatrics 2011;49(8):626-630
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo identify thyroid peroxidase (TPO) gene mutations in 35 patients with congenital hypothyroidism.
METHODGenomic DNA was isolated from peripheral blood samples of 35 patients with congenital hypothyroidism. All of the 17 exons and flanking introns of TPO gene were amplified by PCR, then the PCR products were sequenced bi-directionally and were analyzed by restriction endonucleases.
RESULTOne patient had compound heterozygous mutations c.961A>G/c.2422delT, one was c.2268insT/c.1477G>A, and three was homozygous mutation c.2268insT. The TPO gene mutation c.961A>G [p. Thr321Ala] was one novel mutation.
CONCLUSIONHigh frequency mutation in TPO gene was detected in patients with congenital hypothyroidism.
