Consultant of
Cardiology and Vascular Disease (Heart)
Consultant heart and coronary catheterization at the National Heart Institute
Consultant of cardiology and blood vessels
Member of the European Society of Cardiology and Catheterization - Member of the Egyptian Society of Cardiology
Professor of
Cardiology and Vascular Disease (Heart)
Consultant of cardiology and catheterization, the general authority and vessels for hospitals and educational institutes. ▪️ Egyptian Fellowship Coach for Cardiology
▪️ Member of the European Society of Cardiology
And the catheter.
▪️ Egyptian fellowship for sound waves on the heart. ▪️ Member of the European Society of Ultrasound on the Heart.
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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.