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Department

About the department

Department name (English):  Pediatrics Department

Department name (original):  Pediatria

Subnetworks of expertise:

  • Myeloid malignancies
  • Bleeding - Coagulation disorders

Healthcare provider: Centro Hospitalar do Porto, EPE

Diseases covered by the department:

  • Rare coagulation disorder
  • Rare hemorrhagic disorder
  • Rare hemorrhagic disorder due to a coagulation factors defect
  • Rare hemorrhagic disorder due to a constitutional coagulation factors defect
  • Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
  • Hemophilia
  • Hemophilia A
  • Hemophilia B
  • Congenital factor V deficiency
  • Congenital fibrinogen deficiency
  • Familial afibrinogenemia
  • Familial dysfibrinogenemia
  • Familial hypofibrinogenemia
  • Familial hypodysfibrinogenemia
  • Congenital alpha2-antiplasmin deficiency
  • Congenital factor XIII deficiency
  • Von Willebrand disease
  • Von Willebrand disease type 1
  • Von Willebrand disease type 2
  • Von Willebrand disease type 3
  • Congenital factor XI deficiency
  • Congenital plasminogen activator inhibitor type 1 deficiency
  • Congenital high-molecular-weight kininogen deficiency
  • Congenital prekallikrein deficiency
  • Combined deficiency of factor V and factor VIII
  • Congenital vitamin K-dependent coagulation factors deficiency
  • Congenital factor VII deficiency
  • Congenital factor II deficiency
  • Congenital factor X deficiency
  • Hereditary combined deficiency of vitamin K-dependent clotting factors
  • Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
  • East Texas bleeding disorder
  • Thrombomodulin-related bleeding disorder
  • Rare hemorrhagic disorder due to an acquired coagulation factor defect
  • Rare hemorrhagic disorder due to a platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional platelet anomaly
  • Rare hemorrhagic disorder due to a constitutional thrombocytopenia
  • Syndromic constitutional thrombocytopenia
  • Isolated constitutional thrombocytopenia
  • Rare hemorrhagic disorder due to a qualitative platelet defect
  • Glanzmann thrombasthenia
  • Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
  • Ehlers-Danlos syndrome, fibronectinemic type
  • Scott syndrome
  • P2Y12 defect
  • Pseudo-von Willebrand disease
  • Bleeding diathesis due to a collagen receptor defect
  • Bleeding disorder due to CalDAG-GEFI deficiency
  • Rare hemorrhagic disorder due to an acquired platelet anomaly
  • Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome
  • TAFRO syndrome
  • HELLP syndrome
  • Fetal and neonatal alloimmune thrombocytopenia
  • Kasabach-Merritt syndrome

Patients covered

  • Pediatrics