Practical Pediatric HematologyAnupam Sachdeva Evidence-based medicine is the need of the hour. Every pediatrician strives for perfection is his or her practice. These are exciting times for Pediatric Hematology and Oncology. Major advances during the past decade in the field have enhanced the understanding and significantly influenced the management and outcome of many of these chronic and fatal diseases affecting children. While opportunities to learn decrease after one leaves the medical school, science keeps evolving. Keeping this in mind, Indian Academy of Pediatrics (IAP) envisaged starting specialty training under its plan of action 2006. Such trainings keep professional and residents updated about newly launched technologies and other advancements. This book is well illustrated and has many pictures and diagrams for the quick understanding of readers. This will be of use not only to the postgraduates of pediatrics but also will be of immense use to a general pediatrician as a ready-reckoner to be kept on the desk. |
From inside the book
Results 1-5 of 61
Page xv
... thalassemia; publishing management guidelines on sickle cell disease, ITP, blood component therapy national training programs on pediatric oncology; publication of PHO newsletter; promoting subspecialty fellowship training; preparing ...
... thalassemia; publishing management guidelines on sickle cell disease, ITP, blood component therapy national training programs on pediatric oncology; publication of PHO newsletter; promoting subspecialty fellowship training; preparing ...
Page xx
... Thalassemia 83 Gene Therapy 83 Hemolytic Anemia (Other than Thalassemia) Management MB Agarwal Hereditary Hemolytic Anemias (Intracorpuscular Defect) 85 Acquired Hemolytic Anemias Chemical Agents Physical Agents Paroxysmal Nocturnal ...
... Thalassemia 83 Gene Therapy 83 Hemolytic Anemia (Other than Thalassemia) Management MB Agarwal Hereditary Hemolytic Anemias (Intracorpuscular Defect) 85 Acquired Hemolytic Anemias Chemical Agents Physical Agents Paroxysmal Nocturnal ...
Page 2
... Thalassemia 5. Postsplenectomy state 6. Hereditary xerocytosis 7. Lecithin cholesterol acyl transferase deficiency (LCAT deficiency). Howell-Jolly Bodies They are nuclear remnants that are not extruded from mature erythrocytes and ...
... Thalassemia 5. Postsplenectomy state 6. Hereditary xerocytosis 7. Lecithin cholesterol acyl transferase deficiency (LCAT deficiency). Howell-Jolly Bodies They are nuclear remnants that are not extruded from mature erythrocytes and ...
Page 3
... thalassemia and lead intoxication. Rouleaux Formation It occurs when plasma proteins block the negative charge on ... Thalassemia trait Iron deficiency Normal Chronic disease -thalassemia Chrds. Hb H Sickle/HbC Hemoglobinop. trait ...
... thalassemia and lead intoxication. Rouleaux Formation It occurs when plasma proteins block the negative charge on ... Thalassemia trait Iron deficiency Normal Chronic disease -thalassemia Chrds. Hb H Sickle/HbC Hemoglobinop. trait ...
Page 5
... Thalassemia Lead poisoning 5. Sideroblastic anemia. 3. 4. Iron deficiency, is a common cause of microcytic anemia in children between 1 and 3 years of age. Iron deficiency may potentiate the toxic effects of lead poisoning; in most ...
... Thalassemia Lead poisoning 5. Sideroblastic anemia. 3. 4. Iron deficiency, is a common cause of microcytic anemia in children between 1 and 3 years of age. Iron deficiency may potentiate the toxic effects of lead poisoning; in most ...
Contents
Chapter21 | 156 |
Chapter22 | 165 |
Chapter23 | 178 |
Chapter24 | 181 |
Chapter25 | 199 |
Chapter26 | 208 |
Chapter27 | 232 |
Chapter28 | 247 |
Chapter09 | 69 |
Chapter10 | 75 |
Chapter11 | 85 |
Chapter12 | 90 |
Chapter13 | 97 |
Chapter14 | 115 |
Chapter15 | 120 |
Chapter16 | 125 |
Chapter17 | 130 |
Chapter18 | 144 |
Chapter19 | 148 |
Chapter20 | 153 |
Chapter29 | 259 |
Chapter30 | 262 |
Chapter31 | 266 |
Chapter32 | 272 |
Chapter33 | 281 |
Chapter34 | 289 |
Chapter35 | 298 |
Chapter36 | 305 |
Chapter37 | 309 |
Index | 313 |
Other editions - View all
Common terms and phrases
abnormalities acid activity acute adults antibodies anticoagulant antigen aplastic anemia APTT assay associated bleeding blood loss bone marrow transplantation catheter cause chemotherapy child childhood chronic clinical concentration congenital cytopenia decreased defects develop diagnosis disease disorders Disseminated intravascular coagulation donor dose drugs erythrocyte erythropoietin factor VIII ferritin fetal fibrin fibrinogen folate g/dl gene globin granulocytes Haematol hematocrit hematological hemoglobin hemolysis hemolytic anemia hemophilia hemorrhage heparin hepatitis immune increased India infants infection infusion inhibitor intravenous iron deficiency ischemic laboratory leukemia levels liver malignancy mutations myelodysplastic syndrome myeloid neonatal neutropenia newborn normal nutritional occur oral patients Pediatr peripheral plasma platelet platelet count platelet transfusion present preterm prophylaxis protein prothrombin red cell reticulocyte count risk serum severe splenectomy stem cell stroke studies syndrome Table thalassemia therapy thrombin thrombocytopenia thrombocytosis thrombosis tissue treatment usually venous viral virus vitamin