The Foundation has intention to have all necessary arrangements and minimal diagnostic units to do the usual tests and the other investigations can be done from local or Kolkata diagnostic centres or elsewhere.
The Foundation can help the needy people to bear their necessary expenses for these tests at the initial stage.
The screening of people or children will be done where ever any doubt exists regarding the possibilities of Hyperoxaluria, Primary or Secondary.
We know that diabetics is the commonest disorder, but there are other cases of metabolic disorder such as hypercalciuria and nephrocalcinosis (FHHNC), and primary hyperoxaluria (PH), which remain undiagnosed in usual treatment. These cases are detected by suitable new diagnostic protocol for further investigation. These special tests include DNA isolation test, nuclear medicine test, cystogram, ultrasonography etc.