ba0003pp410 | Paediatric bone disease | ECTS2014
Schundeln Michael
, Goretzki Sarah
, Hauffa Pia
, Marschke Laura
, Wieland Regina
, Bauer Jens
, Hauffa Berthold
, Grasemann Corinna
Introduction: Bone health in patients with sickle cell disease and thalassemia is impaired. These patients feature altered parameters of bone metabolism and bone mineral density.Aim and design: To investigate bone health in patients with hemolytic anemia we conducted a cross-sectional analysis in our Hematology Outpatient Clinic at the Childrens Hospital Essen. The largest subgroups within our cohort are patients with homozygous sickle cell (HBSS) ...