DMAP1 Syndrom

Today we are in Berlin attending the conference NAKSE (Nationale Konferenz zu seltenen Erkrankungen). This is a good opportunity for exchange and collaboration related to rare diseases and pay also more attention for DMAP1.

We have received approval from „Ministe-
rium für Arbeit, Gesundheit und Soziales des Landes Nordrhein-Westfalen (MAGS)“ for the funding measure „Inklusionsscheck“ for our association DMAP1 Syndrom e.V. Together with .textil and www.schatzitsystems.de we will finalize our website www.dmap1.de and make it accessible, as well as create initial information material about this extremely rare genetic defect.