Coexistence of Gitelman's syndrome and thyroid disease: SLC12A3 gene analysis in two patients / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
;
(12): 395-398, 2010.
Artículo
en Chino
| WPRIM
| ID: wpr-389647
ABSTRACT
Two patients with coexistence of thyroid disease and suspected Gitelman's syndrome underwent SLC12A3 gene analysis. The results confirmed that both patients were compound heterozygotes of SLC12A3 gene mutation. Three novel variants of SLC12A3 were found in this study. This report suggests that Gitelman's syndrome may coexist with other disorders associated with hypokalemia, such as Graves' disease.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Idioma:
Chino
Revista:
Chinese Journal of Endocrinology and Metabolism
Año:
2010
Tipo del documento:
Artículo
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