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Bento, Celeste

About me

Name: Celeste

Surname: Bento

Academic title: Clinical Laboratory Geneticist


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

  • Diagnostics

Diseases:

Rare anemia Hemoglobinopathy Hemoglobin E disease Hemoglobin D disease Unstable hemoglobin disease Alpha-thalassemia and related diseases Alpha-thalassemia Hemoglobin H disease Hb Bart's hydrops fetalis Alpha-thalassemia-related diseases Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Alpha-thalassemia-myelodysplastic syndrome Beta-thalassemia and related diseases Beta-thalassemia Beta-thalassemia major Beta-thalassemia intermedia Dominant beta-thalassemia Beta-thalassemia associated with another hemoglobin anomaly Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Delta-beta-thalassemia Hemoglobin C-beta-thalassemia syndrome Hemoglobin E-beta-thalassemia syndrome Hemoglobin Lepore-beta-thalassemia syndrome Beta-thalassemia with other manifestations Beta-thalassemia-X-linked thrombocytopenia syndrome Sickle cell disease and related diseases Sickle cell anemia Sickle cell disease associated with an other hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Hemoglobinopathy Toms River Hereditary methemoglobinemia Hemoglobin C disease Hemoglobin M disease Rare hemolytic anemia Rare constitutional hemolytic anemia Rare constitutional hemolytic anemia due to a red cell membrane anomaly Hereditary spherocytosis Hereditary elliptocytosis Hereditary stomatocytosis Overhydrated hereditary stomatocytosis Dehydrated hereditary stomatocytosis Southeast Asian ovalocytosis Rare constitutional hemolytic anemia due to an enzyme disorder Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies Hemolytic anemia due to glutathione reductase deficiency Hemolytic anemia due to a disorder of glycolytic enzymes Triose phosphate-isomerase deficiency Hemolytic anemia due to red cell pyruvate kinase deficiency Hemolytic anemia due to glucophosphate isomerase deficiency Hemolytic anemia due to diphosphoglycerate mutase deficiency Non-spherocytic hemolytic anemia due to hexokinase deficiency Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Class I glucose-6-phosphate dehydrogenase deficiency Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Hemolytic anemia due to adenylate kinase deficiency Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Heinz body anemia

Which is your patient age coverage?

  • Pediatrics
  • Adults
  • Ageing


Member Go to member

Name english: Centro Hospitalar e Universitário de Coimbra, EPE

Name original: Centro Hospitalar e Universitário de Coimbra, EPE


Healthcare provider Go to healthcare provider

Name english: Centro Hospitalar e Universitário de Coimbra, EPE

Name original: Centro Hospitalar e Universitário de Coimbra, EPE

Departments

English name Original name Subnetworks of expertise Healthcare provider