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Sickle Cell Disease is a common hereditary form of anaemia. The disease leads to chronic anaemia and pain caused by the occlusion of small blood vessels due to sickle shaped red blood cells. This leads to severe complications and organ damage, resulting in reduced life expectancy. Charlotte van Tuin evaluates the frequency of pain and looks at the best way to combat this through hospitalisation. She also researches the prevalence and progression levels of various forms of organ damage.

Event details of Pain burden in Sickle Cell Disease
Date 29 June 2018
Time 12:00
Location Agnietenkapel
Room Location

C.F.J. van Tuijn: Sickle Cell Disease. Evaluation and Management of Disease Burden.

Supervisor

Prof. M.H.J. van Oers.

Co-supervisor

B.J. Biemond

Agnietenkapel

Room Location

Oudezijds Voorburgwal 229 - 231
1012 EZ Amsterdam

Entrance

This event is open to the public.