Fondazione Italiana Sindromi Mielodisplastiche-ETS
Development of an Italian regional registries MDS network using the same electronic case report form for data storage, with the following broad aims:
* Ability to aggregate and process anonymous epidemiological data collected by individual regional registers;
* Ability to aggregate the available data with those of other international registries existing.
Age
18–106
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
New diagnosis of MDS
You may not be if
Patient who refuse the signature of informed consent
