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