Experts

Information

Mikael Sundin

About me

Name: Mikael

Surname: Sundin

Academic title: Associate Professor

Charge: Clinical Director/Senior Consultant Pediatric Hematology-Oncology

Link to personal website:

https://ki.se/en/people/miksun


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

  • Diagnostics
  • Treatment and care

Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):

Allogeneic hematopoietic cell transplantation (HCT), pediatric non-malignant hematology (especially BMFs) , pediatric myelodysplastic syndromes and myeloproliferative disorders (i.e., PV, ET and KML), primary immunodeficiency with hematologic manifestations and WGS as a diagnostic tool in hematology/immunology.

Diseases:

Hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome” , Thrombocytopenia with congenital dyserythropoietic anemia , X-linked dyserythropoetic anemia with abnormal platelets and neutropenia , Autosomal thrombocytopenia with normal platelets , Congenital amegakaryocytic thrombocytopenia , Rare anemia , Hemoglobinopathy , Hemoglobin E disease , Hemoglobin D disease , Unstable hemoglobin disease , Alpha-thalassemia and related diseases , Alpha-thalassemia , Alpha-thalassemia-related diseases , Beta-thalassemia and related diseases , Beta-thalassemia , Beta-thalassemia associated with another hemoglobin anomaly , Beta-thalassemia with other manifestations , Sickle cell disease and related diseases , Sickle cell anemia , Sickle cell disease associated with an other hemoglobin anomaly , Hemoglobin C disease , Hemoglobin M disease , Rare hemolytic anemia , Rare constitutional hemolytic anemia , Rare constitutional hemolytic anemia due to a red cell membrane anomaly , Rare constitutional hemolytic anemia due to an enzyme disorder , Heinz body anemia , Rare acquired hemolytic anemia , Aplastic anemia , Rare constitutional aplastic anemia , Blackfan-Diamond anemia , Dyskeratosis congenita , Fanconi anemia , Revesz syndrome , Hoyeraal-Hreidarsson syndrome , WT limb-blood syndrome , Shwachman-Diamond syndrome , Autosomal dominant aplasia and myelodysplasia , Hereditary isolated aplastic anemia , Pancytopenia-developmental delay syndrome , Rare acquired aplastic anemia , Idiopathic aplastic anemia , Red cell aplasia , Monocytopenia with susceptibility to infections , Rare deficiency anemia , Constitutional deficiency anemia , Constitutional dyserythropoietic anemia , Congenital dyserythropoietic anemia , Congenital dyserythropoietic anemia type I , Congenital dyserythropoietic anemia type III , Congenital dyserythropoietic anemia type II , Congenital dyserythropoietic anemia type IV , Pancreatic insufficiency-anemia-hyperostosis syndrome

Which is your patient age coverage?

  • Pediatrics


Member Representative

Subnetwork representative:

  • Red blood cell
  • Bone marrow failure

Member Go to member

Name english: Karolinska University Hospital

Name original: Karolinska Universitetssjukhuset


Healthcare provider Go to healthcare provider

Name english: Karolinska University Hospital

Name original: Karolinska Universitetssjukhuset

Departments

English name Original name Subnetworks of expertise Healthcare provider

Euro Blood Net