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

Lignende værker

• A case of Gitelman syndrome: our experience with a patient treated in clinical practice on a local island
  af: Chinen, Takashi, et al.
  Udgivet: (2019)
• Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous Mutation
  af: Kusuda, Takeshi, et al.
  Udgivet: (2016)
• HPRT-related hyperuricemia with a novel p.V35M mutation in HPRT1 presenting familial juvenile gout
  af: Mishima, Eikan, et al.
  Udgivet: (2020)
• Exonic Mutations in the SLC12A3 Gene Cause Exon Skipping and Premature Termination in Gitelman Syndrome
  af: Takeuchi, Yoichi, et al.
  Udgivet: (2015)
• Acquired Gitelman Syndrome
  af: Kim, Yong Kyun, et al.
  Udgivet: (2009)