Orphanet Polska - w europejskiej sieci jako szansa oceny sytuacji chorób rzadkich na przykładzie wrodzonych wad metabolizmu u dzieci

The authors present unsolved problem of rare diseases in Poland on the example of inborn errors of metabolism, with regard to a necessity of dissemination of common definition of these diseases, a preparation of multithread expert opinion and introduction of systemic solutions in the health care. An active Poland participation in the European project Orphanet is a chance for this process acceleration. A justification of bringing a national programme concerning rare diseases into being, requires a penetrating analysis.