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Inherited, not acquired, Gitelman syndrome in a patient with Sjögren’s syndrome: importance of genetic testing to distinguish the two forms

Gitelman syndrome (GS) is an autosomal recessive, salt-losing renal tubulopathy caused by mutations in the SLC12A3 gene; however, it can also be acquired in patients with autoimmune disease, especially in those with Sjögren’s syndrome. Differentiating between the inherited and acquired forms of GS i...

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Détails bibliographiques
Publié dans:CEN Case Rep
Auteurs principaux: Mishima, Eikan, Mori, Takayasu, Sohara, Eisei, Uchida, Shinichi, Abe, Takaaki, Ito, Sadayoshi
Format: Artigo
Langue:Inglês
Publié: Springer Singapore 2017
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5694408/
https://ncbi.nlm.nih.gov/pubmed/28819721
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-017-0271-4
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