Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired disease characterized by intravascular hemolysis and hemoglobinuria. Leukopenia, thrombocytopenia, arterial and venous […]

Hemoglobinopathy is a hereditary or congenital change or violation of the structure of the hemoglobin protein, usually leading to clinically […]

The leading Israeli clinic Tel Aviv Medical Clinic uses an innovative approach in the treatment of aplastic anaemia using the […]

Doctors of the leading Israeli clinic Tel Aviv Medical Clinic are engaged in the detection and treatment of diseases of […]

It is extremely rare for people to come to a consultation with a hematologist, since symptoms that can talk about […]

The syndrome of inherited bone marrow failure in children includes Schwachman-Diamond syndrome. It is a rare hereditary disease with an […]

Paroxysmal nocturnal hemoglobinuria is an acquired disease that leads to premature death and impaired blood cell production. The disease affects […]

Thalassemia is a group of congenital microcytic hemolytic anaemia that is characterized by a defect in haemoglobin synthesis. Beta-thalassemia is […]

Sickle cell anaemia is a severe hereditary disease also known as drepanocytosis, meniscocytosis, S-hemoglobin disease, Gerrick syndrome, African hemolytic anaemia. […]

Neutropenia is a disease of the hematopoietic system, which is characterized by a decrease in the number of neutrophils (white […]