Sickle cell registry

The primary goal of the registry is to record the type, complications and treatment of sickle cell disease. In addition, data is provided for scientific analysis. Based on the results, the treatment guideline should be adapted and the care of sickle cell patients thereby improved. The registry is headed by Dr. Joachim Kunz.

Contact:

Dr. med. Joachim Kunz

Im Neuenheimer Feld 430
69120 Heidelberg
Telefon +49 (6221) 563 9836
joachim.kunz(at)med.uni-heidelberg.de

Further information on the sickle cell registry can be found on the GPOH hematology study protocol.