The study of SLC12A3 complicated heterozygotic mutation in Children Gitelman syndrome
- VernacularTitle:儿童 Gitelman 综合征的 SLC12 A3基因复杂杂合突变
- Author:
Chunlin GAO
;
Shangru MA
;
Zhengkun XIA
;
Yuanfu GAO
;
Zhongmin FAN
;
Min XU
;
Wei WEI
;
Yu ZHOU
;
Guiling MO
- Publication Type:Journal Article
- Keywords:
Gitelman Syndrome;
Children;
SLC12 A3 gene
- From:
Journal of Medical Postgraduates
2015;(1):37-40
- CountryChina
- Language:Chinese
-
Abstract:
Objective Gitelman Syndrome is a disease caused by the mutation of Na-Cl cotransporter gene(SLC12A3).The article studied the significance of diagnosis and identification by genetic mutation. Methods We collected the clinical data, then we sequenced the SLC12A3 gene by the first sequencing technology and MLPA. Results SLC12A3 complicated heterozygotic mutation was observed.One of them showed c.1964G>A, p.(Arg655His) and exon 8 deletion mutation, the other showed c.2543A>T, p.(Asp848Val) and c.976delG, p.(Val326fs) mutation of SLC12A3 gene in children. Conclusion The final diagnosis depended on gene diagnosis. Pediatrician must recognize the manifestations to advoid misdiagnosis.
