Members

Name: Paul

Surname: Brons

Academic title: MD PhD

Which is your area of expertise for the "Disease/group of diseases"?

• Diagnostics
• Treatment and care

Disease groups:

Acquired idiopathic sideroblastic anemia Atypical hemolytic-uremic syndrome Constitutional sideroblastic anemia (excluding Severe congenital hypochromic anemia with ringed sideroblasts) Hemophilia A Hemophilia B Hereditary Hyperferritinemia with or without cataract (OMIM 600886) HFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1 - OMIM 235201) Iron-refractory iron deficiency anemia syndrome Microcytic anemia with liver iron overload Myelodysplastic syndrome Myeloproliferative neoplasm (Other than Chronic myeloid leukemia and Primary myelofibrosis) Neuroferritinopathy Rare acquired deficiency anemia (Plummer-Vinson syndrome) Rare constitutional aplastic anemia (Other than BDA, DKC, FA, SDS) Rare hemorrhagic disease due to constitutional coagulation factors defects (Other than Hemophilia and Von Willebrand disease) Rare hemorrhagic disorder due to a constitutional platelet anomaly Rare hemorrhagic disorder due to an acquired platelet anomaly Rare hereditary hemochromatosis (Other than Type 1) Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to quantitative platelet anomaly (High) Rare thrombotic disorder due to quantitative platelet anomaly (Low) Severe congenital hypochromic anemia with ringed sideroblasts Typical hemolytic-uremic syndrome Von Willebrand disease

Which is your patient age coverage?

• Pediatrics