Article Text
Research Article
Non-psychogenic primary polydipsia in autoimmune chronic active hepatitis with severe hyperglobulinaemia.
Abstract
The association of hyperglobulinaemia with renal tubular acidosis and nephrogenic diabetes insipidus is well established. A patient with marked hyperglobulinaemia due to autoimmune chronic active hepatitis is described who presented with severe polydipsia and polyuria but had entirely normal renal tubular function indicating a primary thirst disorder.