Professor and Senior Consultant of Rheumatology, Joint Diseases and Immunology
Member of the European, American and Arab Society of Rheumatology, the International Association for Rheumatology, the Egyptian Society of Rheumatic Diseases, the Egyptian Society of Osteoporosis, the Egyptian Society of Arthritis, the Egyptian Back Pain Society.
Rheumatology and Rehabilitation Consultant.
* Instructor, Faculty of Medicine, Ain Shams University.
* Treatment of all rheumatic and immune diseases.
*Treatment of joint and spine pain.
*Treatment of osteoporosis and joint stiffness.
* Joint injections, tendonitis and ligaments.
PhD of Rheumatology and Clinical Immunology - Cairo University Consultant of Rheumatology , Immunology and Joint Diseases Lecturer of Rheumatology and Immune Diseases - Kasr Aini
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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.