low platelet count thrombocytopenia
Conditions
Interventions
None listed
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
2 Years to 64 Years
Inclusion criteria
Inclusion criteria: Part 1: Patients diagnosed with Lowe syndrome All ages Part 2: Patients diagnosed with AML After first remission induction (RI) cycle In complete remission after first RI cycle
Exclusion criteria
Exclusion criteria: Part 1: patients with a known bleeding disorder Unwilling to give informed consent Patients using anticoagulants Part 2: patients receiving platelet transfusion in the study period unwilling to give informed consent Patients using anticoagulants
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| For Part 1 as well as Part 2: platelet characteristics using staining of alpha tubulin and VWF and SPARC. | — |
Countries
Netherlands
Outcome results
None listed