Experts

Information

Gian Luca Forni

About me

Name: Gian Luca

Surname: Forni

Academic title: Medical Doctor

Charge: Director


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

  • Prevention and genetic counseling
  • Diagnostics
  • Treatment and care

Diseases:

Acquired idiopathic sideroblastic anemia , Rare anemia , Sideroblastic anemia , Constitutional sideroblastic anemia , Pearson syndrome , Mitochondrial myopathy and sideroblastic anemia , X-linked sideroblastic anemia and ataxia , Thiamine-responsive megaloblastic anemia syndrome , X-linked sideroblastic anemia , Adult-onset autosomal recessive sideroblastic anemia , Autosomal recessive sideroblastic anemia , Severe congenital hypochromic anemia with ringed sideroblasts , Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome , 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 , Hemoglobinopathy Toms River , Hereditary methemoglobinemia , Hemoglobin C disease , Hemoglobin M disease , Acquired methemoglobinemia , 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 deficiency anemia , Constitutional deficiency anemia , Constitutional anemia due to iron metabolism disorder , Rare acquired deficiency anemia , Plummer-Vinson syndrome , Rare hereditary hemochromatosis , HFE related hereditary hemochromatosis , Symptomatic form of hemochromatosis type 1 (OMIM 235200) , Hemochromatosis due to rare mutations in HFE (OMIM 235200) , Non-HFE related hereditary hemochromatosis , Hemochromatosis type 2(OMIM 602390, 613313) , Hemochromatosis type 2A (OMIM 602390) , Hemochromatosis type 2B (OMIM 613313) , Hemochromatosis type 3 (OMIM 604250) , Hemochromatosis type 5 (OMIM 615517) , Hemochromatosis type 4B (OMIM 606069) , Ferroportin Disease , Hemochromatosis type 4A (OMIM 606069)

Which is your patient age coverage?

  • Pediatrics
  • Adults
  • Ageing


Member Representative

Member Go to member

Name english: E.O. Ospedali Galliera, Genova

Name original: E.O. Ospedali Galliera, Genoa


Healthcare provider Go to healthcare provider

Name english: E.O. Ospedali Galliera, Genova

Name original: E.O. Ospedali Galliera, Genoa

Departments

English name Original name Subnetworks of expertise Healthcare provider

Euro Blood Net