Familial hypokalaemia - hypomagnesaemia (Q99736)

From determinar.ia.br - Determine suas informações
Revision as of 16:24, 16 August 2026 by Determinaradmin (talk | contribs) (‎Changed an Item)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Gitelman syndrome, also referred to as familial hypokalaemia-hypomagnesemia, is a genetic renal tubular disease characterised by hypokalaemia metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion.
Language Label Description Also known as
default for all languages
ID_1177986055
    English
    Familial hypokalaemia - hypomagnesaemia
    Gitelman syndrome, also referred to as familial hypokalaemia-hypomagnesemia, is a genetic renal tubular disease characterised by hypokalaemia metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion.

      Statements

      CID11:ID_1177986055
      0 references
      dki-india-ID_1177986055
      0 references
      Concluído
      0 references
      15 August 2026
      0 references