Deutsche Interessengemeinschaft für Phenylketonurie

This site uses cookies. By continuing to browse this site, you are agreeing to our Cookie Policy.

  • The DIG-PKU was founded 1975 by 8 parents, whose kids have PKU. Until today there are about 1550 members on the DIG-PKU. The main objective is to care for PKU as well as other inborn errors. The DIG-PKU is divided into 16 local groups as well as four groups for "Organoacidämien", "Harnstoffzyklusstörungen", "NKH" and "Tyrosinose".
    Website: dig-pku.de

    2,251 times viewed