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Leblanc, Thierry

About me

Name: Thierry

Surname: Leblanc


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

  • Prevention and genetic counseling
  • Diagnostics
  • Treatment and care

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

Diagnostic and care of patients with inherited bone marrow failure syndromes and acquired aplastic anemias.

Diseases:

Primary myelofibrosis 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 Evans syndrome STAT3-related early-onset multisystem autoimmune disease Rare anemia Thiamine-responsive megaloblastic anemia syndrome Severe congenital hypochromic anemia with ringed sideroblasts Rare hemolytic anemia Rare acquired hemolytic anemia Paroxysmal nocturnal hemoglobinuria Typical hemolytic-uremic syndrome Autoimmune hemolytic anemia Autoimmune hemolytic anemia, cold type Cold agglutinin disease Paroxysmal cold hemoglobinuria Autoimmune hemolytic anemia, warm type Mixed-type autoimmune hemolytic anemia Drug-induced autoimmune hemolytic anemia Hemolytic disease due to fetomaternal alloimmunization Hemolytic disease of the newborn with Kell alloimmunization 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 Transient erythroblastopenia of childhood Adult pure red cell aplasia Monocytopenia with susceptibility to infections Rare deficiency anemia Constitutional deficiency anemia Constitutional anemia due to iron metabolism disorder Congenital atransferrinemia Aceruloplasminemia Microcytic anemia with liver iron overload IRIDA syndrome Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder Methylmalonic acidemia with homocystinuria Methylmalonic acidemia with homocystinuria, type cblC Methylmalonic acidemia with homocystinuria, type cblD Methylmalonic acidemia with homocystinuria type cblF Methylmalonic acidemia with homocystinuria, type cblJ Methylmalonic acidemia with homocystinuria, type cblX Transcobalamin deficiency Congenital intrinsic factor deficiency Homocystinuria without methylmalonic aciduria Methylcobalamin deficiency type cblE Methylcobalamin deficiency type cblG Methylcobalamin deficiency type cblDv1 Gräsbeck-Imerslund disease Constitutional megaloblastic anemia due to folate metabolism disorder Formiminoglutamic aciduria Hereditary folate malabsorption Constitutional megaloblastic anemia with severe neurologic disease Vitamin B12- and folate-independent constitutional megaloblastic anemia Hereditary orotic aciduria Hypoxanthine-guanine phosphoribosyltransferase deficiency Lesch-Nyhan syndrome Hypoxanthine guanine phosphoribosyltransferase partial deficiency 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

Which is your patient age coverage?

  • Adults


Member Go to member

Name english: Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis

Name original: Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Louis


Healthcare provider Go to healthcare provider

Name english: Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré

Name original: Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré

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English name Original name Subnetworks of expertise Healthcare provider