We observed severe overhydration in an 18-month-old Japanese girl with prim
ary polydipsia. The secretion of antidiuretic hormone (ADH) was decreased,
and urinary excretion of aquaporin-2, a vasopressin-sensitive water channel
protein, was suppressed under basal conditions, but the response of aquapo
rin-2 to ADH was essentially preserved. These findings suggest that the wat
er channel itself was intact and that overhydration resulting from polydips
ia was responsible for the decreased ADH secretion and suppression of the w
ater channel protein.