Professor of Oncology, Hematology and Marrow Transplantation - National Cancer Institute - Cairo University Consultant of Oncology, Hematology and Marrow Transplantation at Dar Al Fouad Hospitals
Consultant of Hematology at Maadi Military Hospital, Ph.D. of Hematology and Hematology, Alexandria Medicine, Master of Hematology and Oncology, Ain Shams University, Member of the Egyptian Group of Hematology and Member of the Military Medical Academy
Professor of Internal Medicine and Hematology - Faculty of Medicine - Ain Shams University. Former Director of the Hematology and Marrow Transplantation Units at Ain Shams University Hospitals
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Yes, a hematologist treats haemorrhage cases and other cases like erythrocyte problems, anaemia, leukemia, lymphoma, autoimmune disorder and genetic blood diseases. .
A hematologist treats any blood related cases, including haemorrhage, erythrocyte problems, anaemia, leukemia, lymphoma, autoimmune disorder and genetic blood diseases
No, it's not the same thing; because leukemia affects white blood cells, not platelets, and white blood cells do not function normally. Blood cancer causes a deficiency in all blood components, including platelets.
Autoimmune diseases are conditions that occur as a result of the immune system's excessive activity, attacking and mistakenly eliminating healthy cells and tissues in the body. Examples include thyroiditis, type 1 diabetes, vasculitis, rheumatoid arthritis, and psoriasis.
It is a chronic disorder resulting from the complete failure of the pancreas to produce insulin, due to the body's immune system attacking and destroying the pancreatic cells (an autoimmune disease). Insulin is a crucial hormone for enhancing the ability of glucose to enter cells and produce energy. Type 1 diabetes causes an elevation in blood glucose levels.
It is a genetic disorder that affects the body's ability to produce hemoglobin and red blood cells, resulting in a decrease in their numbers, and causing the red blood cells to become extremely small in size.
Sickle cell anemia is a hereditary disease (HBS) that is passed from parents to children through genetic inheritance. Genes, which determine the characteristics of the body, are responsible for this condition. Each person has a pair of genes that specify the type of hemoglobin. Sickle cell anemia is entirely different from regular anemia, which occurs due to a deficiency in the hemoglobin levels in the blood.
