[Bartter's disease associated with hypercorticism, phosphate and magnesium deficiencies and familial renal tubular disease]. / Un syndrome de bartter associant un hypercortisolisme, un diabete phosphore et magnesien et une tubulopathie d'origine familiale

A new case of Bartter's syndrome is described. There is a context of other cases of familial renal tubular disease with a sex-linked heredity. In this case, the Bartter's syndrome is associated with magnesium deficiency and hypomagnesemia, with a ricket and severe phosphate deficiency, and finally with an hypercorticism. The basal secretion rate of cortisol agree with a Cushing's syndrome. This hypercorticism is corrected by aminogluthetimide. The influence of the hyperreninism on the hypercorticism is discussed.