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19thGlobal Summit on Hematology and Infectious Diseases, will be organized around the theme “Theme: Surveying Recent Outbreaks, Technologies and Research in Infectious Disease Treatment”

Blood Disorders 2023 is comprised of 21 tracks and 0 sessions designed to offer comprehensive sessions that address current issues in Blood Disorders 2023.

Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.

Register now for the conference by choosing an appropriate package suitable to you.

Haematological cancer, commonly known as blood cancer, develops when abnormal blood cells proliferate out of control. The aberrant cells may push away healthy blood cells, which are crucial to the body's operation: Oxygen is helped to go throughout the body by red blood cells. Infections are fought off by white blood cells.

Leukaemia, lymphoma, and myeloma are common forms of hematopoietic malignancy.
 
  • Track 1-1Advances in the Diagnosis and Treatment of Acute Leukemia
  • Track 1-2Novel Therapies for Chronic Lymphocytic Leukemia
  • Track 1-3Current Challenges in Multiple Myeloma Treatment
  • Track 1-4Emerging Therapies for Non-Hodgkin Lymphoma
  • Track 1-5Advances in Hemophilia Management

Hemostasis and thrombosis are two closely connected processes that are essential to the body's capacity to keep blood flowing and stop bleeding.

A blood clot (thrombus) that forms inside a blood artery and can either totally or partially impede blood flow is referred to as thrombosis. Serious medical disorders such deep vein thrombosis, pulmonary embolism, stroke, and heart attack can result from this.

On the other side, hemostasis describes the body's innate capacity to halt bleeding following an accident or damage to a blood artery. Blood vessel constriction, platelet activation and aggregation, and the creation of a fibrin clot to close the wound are all processes in the hemostatic process.

  • Track 2-1Diagnosis and Management of Venous Thromboembolism
  • Track 2-2Platelet Disorders: From Diagnosis to Treatment
  • Track 2-3Thrombotic Microangiopathies: New Insights and Treatment Approaches

A category of medical illnesses known as bleeding disorders cause excessive or protracted bleeding after an accident or surgery because the blood cannot clot correctly. There are two primary categories of bleeding disorders:

Haemophilia is a clotting factor VIII (haemophilia A) or IX (haemophilia B) deficiency-related hereditary bleeding condition.

vWD, or von Willebrand disease This is the most prevalent hereditary bleeding condition and is brought on by a lack of or malfunction in the protein known as von Willebrand factor, which is essential for platelet activity and clotting.

Other bleeding conditions include coagulation factor deficits, such as factor XI deficiency, and platelet diseases include immune thrombocytopenia (ITP) and thrombotic thrombocytopenic purpura (TTP).

  • Track 3-1Diagnosis and Treatment of von Willebrand Disease
  • Track 3-2Factor Replacement Therapy in Hemophilia
  • Track 3-3New Therapies for Rare Bleeding Disorders
  • Track 3-4Inherited Platelet Disorders: Clinical Features and Management

In the medical technique known as hematopoietic stem cell transplantation (HSCT), healthy stem cells are used to replace sick or damaged bone marrow. Both a donor and a patient's own body can provide stem cells for HSCT (allogeneic transplant) or the patient's own body (autologous transplant).

In order to treat or cure illnesses like leukaemia, lymphoma, and other blood-related disorders, HSCT aims to supply fresh, healthy stem cells that can create new blood cells.

HSCT comes in a variety of forms, such as myeloablative and non-myeloablative transplants. In contrast to non-myeloablative transplants, myeloablative transplants employ greater dosages of chemotherapy and radiation therapy.

Infection, graft-versus-host disease (GVHD), and organ damage are a few of the serious hazards and adverse effects of HSCT.

  • Track 4-1Allogeneic Transplantation: Current Practices and Future Directions
  • Track 4-2Haploidentical Transplantation: Advancements and Challenges
  • Track 4-3Umbilical Cord Blood Transplantation: Expanding the Donor Pool
  • Track 4-4CAR T-Cell Therapy for Hematologic Malignancies: Progress and Challenges
Gene and cell therapies are cutting-edge medical procedures that alter the patient's genetic makeup or cells in an effort to treat or improve blood diseases.
 
Gene therapy includes adding new genes or altering existing genes to treat genetic mutations that result in blood problems. To do this, the new genetic material might be introduced into the patient's cells via viruses or other vectors. Inherited blood diseases including sickle cell disease and beta-thalassemia have showed potential for treatment with gene therapy.
 
In cell therapy, damaged cells in the body are replaced or repaired using healthy cells, such as immune or stem cells. For instance, cell treatment known as hematopoietic stem cell transplantation (HSCT) has been utilised for many years to treat certain blood illnesses. New cell treatments have been developed in recent years, such as chimeric antigen receptor (CAR) T-cell therapy, which alters the immune system of a patient to target cancer cells.
 

 

  • Track 5-1Gene Editing for Hemoglobinopathies
  • Track 5-2CAR T-Cell Therapy for Hematologic Malignancies
  • Track 5-3Gene Therapy for Inherited Bleeding Disorders
  • Track 5-4Cell-Based Therapies for Thrombotic Disorders
A set of illnesses known as rare blood disorders often afflict fewer than 1 in 2000 people, representing a tiny fraction of the population. The production, performance, or lifetime of blood cells, including red blood cells, white blood cells, and platelets, can be impacted by several hereditary or acquired illnesses.
 
Examples of rare blood conditions include:
 
1. A hereditary illness called haemophilia weakens the blood's capacity to clot, which causes protracted bleeding episodes.
 
2. A uncommon condition known as aplastic anaemia occurs when the bone marrow is unable to make enough new blood cells.
 
3. Hemolytic anaemia and associated difficulties are brought on by the unusual acquired condition known as paroxysmal nocturnal hemoglobinuria (PNH), in which the body's immune system assaults red blood cells.
 
4. A uncommon condition called thrombotic thrombocytopenic purpura (TTP) causes blood clots to develop in tiny blood capillaries all over the body, which lowers platelet counts and damages organs.
 
5. Hereditary spherocytosis is a hereditary condition that results in spherical red blood cells as opposed to disc-shaped ones, which causes anaemia, jaundice, and an enlarged spleen.

 

  • Track 6-1Diagnosis and Management of Rare Anemias
  • Track 6-2Rare Coagulation Factor Deficiencies: Diagnosis and Treatment
  • Track 6-3Emerging Therapies for Paroxysmal Nocturnal Hemoglobinuria (PNH)

Immunotherapy is a sort of treatment that harnesses the immune system of the patient to combat illnesses, particularly blood problems. It entails the use of medications or other substances to enhance the immune system's capacity to spot and eliminate cancer cells or other aberrant cells.

Immunotherapy has showed promise in the treatment of several malignancies, including leukaemia and lymphoma, in the area of blood disorders. Chimeric antigen receptor (CAR) T-cell treatment is one sort of immunotherapy that has been effective in treating certain blood malignancies. This entails directing a patient's own immune cells, known as T-cells, to seek out and eradicate cancer cells.
 
  • Track 7-1Immune Checkpoint Inhibitors in Hematologic Malignancies
  • Track 7-2Monoclonal Antibodies for Hematologic Malignancies
  • Track 7-3CAR T-Cell Therapy for Multiple Myeloma
  • Track 7-4Novel Approaches to Immunotherapy for Bleeding Disorders

Hematologic illnesses include extremes in cellular component problems, insufficiencies or damage, and dysfunction. Neurologic impairment may be caused by the majority of diseases. Some of these issues are extremely exclusive to the hematologic complaint anaemia, while others are widespread. Hematologic illnesses and the related neurologic conditions are the topic of this session.

  • Track 8-1Thrombocytopenia
  • Track 8-2Cerebra Venous Thrombosis
  • Track 8-3Thalassemia with paraplegia
  • Track 8-4Leptomeningeal metastasis
  • Track 8-5Hypercoagubility and ischemic stroke
  • Track 8-6Ovarian Hyperstimulation Syndrome
  • Track 8-7Polyneuropathy associates with leukoencephalopathy


The science used to treat cancer and other diseases including blood abnormalities is called hematology-oncology (oncology). Additionally, it heals blood malignancies, various diseases such iron deficiency anaemia and thalassemia, as well as tumours of other organs. The course of treatment for a person with myeloma will vary depending on a number of variables. In the case of multiple myeloma, this includes a time known as the smouldering stage, in which there are no obvious symptoms and the myeloma cells in the body are not progressing.


  • Track 9-1Acute myelogenous leukaemia.
  • Track 9-2Non-Hodgkin’s lymphomas
  • Track 9-3Chronic lymphocytic leukaemia
  • Track 9-4Acute lymphoblastic leukaemia
  • Track 9-5Acute monocytic leukaemia
  • Track 9-6Hodgkin’s lymphomas
The study of blood-related difficulties in COVID-19 individuals who have the SARS-CoV-2 virus infection is referred to as haematology. It has been discovered that COVID-19 has a variety of effects on the blood system, including irregular blood coagulation, anaemia, and low platelet counts.
In severe COVID-19 patients, abnormal blood clotting is a frequent consequence that can result in life-threatening conditions including stroke and pulmonary embolism. These patients' care may involve haematologists, who may prescribe anticoagulant medications to stop blood clotting.
 
COVID-19 can also cause anemia, a condition in which there is a deficiency of red blood cells, which can lead to fatigue, weakness, and shortness of breath. Hematologists may perform blood transfusions or prescribe medications to treat anemia in COVID-19 patients.
 
Low platelet counts, a condition known as thrombocytopenia, have also been reported in some COVID-19 patients. This can lead to an increased risk of bleeding and may require platelet transfusions or other treatments.
 
 
  • Track 10-1Hematologic Manifestations of COVID-19
  • Track 10-2Coagulopathy in COVID-19 Patients
  • Track 10-3COVID-19 and Hematopoietic Stem Cell Transplantation
  • Track 10-4Impact of COVID-19 on the Diagnosis and Management of Hematologic Malignancies
Paediatric haematology deals with the research and care of blood diseases in kids, such as those that affect the red blood cells, white blood cells, platelets, and clotting components.
 
Paediatric haematologists are qualified to identify and manage a variety of childhood blood diseases, such as anaemia, haemophilia, sickle cell disease, thrombocytopenia, and leukaemia. They collaborate extensively with other medical specialists to offer complete treatment for kids with complicated blood problems, including paediatric oncologists and geneticists.
 
 
  • Track 11-1Diagnosis and Treatment of Hematologic Malignancies in Children
  • Track 11-2Management of Bleeding Disorders in Children
  • Track 11-3Pediatric Thrombosis and Hemostasis
  • Track 11-4Gene Therapy and Cell Therapy for Pediatric Blood Disorders

Protein biomarkers are particularly useful for identifying breast growth and can be used as biomarkers for early tumour localization. Symptomatic an underlying CT sweep will be performed on patients with probable pancreatic cancer to see whether a tumour may be surgically contained and removed. By performing an H&E neurotic examination, it will be established that 63% of patients have stage III or stage IV illnesses that are not treatable, and a biopsy will be attempted to confirm pancreatic disease. 

  • Track 12-1Drug Targeting
  • Track 12-2Prognosis and treatment production
  • Track 12-3Pharmacodynamics and Pharmacokinetics
  • Track 12-4Monitoring treatment response


The field of hematology known as immunohematology, commonly known as blood management, examines antigen-counteracting agent responses and comparative studies as they relate to the pathophysiology and clinical symptoms of blood issues. Those who operate in this area are known as immuno-hematologists. Cross-coordinating, blood writing, and immune response identifiable proof are among their standard requirements. This area oversees the planning of blood donations, blood components, and other beneficial blood transfusion segments. Due to prior exposure to RBCs from other individuals, as frequently as feasible through pregnancy or transfusion, individuals may have developed a resistance to RBCs. 



Reports of clinical and experimental work in the disciplines of clinical chemistry, hematology, immunology, cancer, and virology are published in Clinical and Experimental Medicine. Clarity, experimental soundness, and knowledge advancements will be the primary evaluation criteria for publications. New clinical or experimental papers that have the potential to influence how clinicians treat patients or think about diseases will be given priority due to their importance now. 



Lack of sufficient numbers of healthy red blood cells to adequately oxygenate the body's tissues is known as Anemia. If you have anaemia, you could feel exhausted and weakened. Anemia can have many different forms, each with a unique aetiology. Anemia can range from mild to severe, and it can be short-term or long-term.


  • Track 15-1Iron deficiency and impaired immunity
  • Track 15-2Iron and pathogens
  • Track 15-3Causes of Anemia
  • Track 15-4Risk factors
  • Track 15-5Nutritional Anemia
  • Track 15-6Stages of Anemia


Myeloma, commonly referred to as multiple myeloma, is a blood cancer that develops from plasma cells. It can be benign or malignant. In the UK, there are approximately 17,500 myeloma patients at any given moment. It is responsible for 2% of all malignancies and 15% of blood cancers. Myeloma primarily affects those over 65, but it has been identified in those as young as 20.


  • Track 16-1Multiple Myeloma
  • Track 16-2Signal Transduction
  • Track 16-3Metastatic Cancer
  • Track 16-4Hematologic Cancer
  • Track 16-5Signaling Pathway
  • Track 16-6Information on Drugs
  • Track 16-7Medicine for Inflammation


The inability of the blood to coagulate (form clots) is known as coagulopathy. This disorder may result in a propensity for prolonged or heavy bleeding, which may happen naturally or after an injury or certain medical and dental procedures.


  • Track 17-1Thrombocytopenia
  • Track 17-2Qualitative Platelet Disorders
  • Track 17-3Inherited Thrombocytopenia
  • Track 17-4Vascular Abnormalities
  • Track 17-5Coagulopathy of liver disease
  • Track 17-6drug-induced platelet dysfunction
  • Track 17-7Acquired clotting factor inhibitors
  • Track 17-8Hemophilia A
  • Track 17-9Hemophilia B


Leukemia is a malignancy that typically develops in the bone marrow, which produces blood. It causes an excess of aberrant white blood cells, a component of the immune system that protects the body from infection, to be produced.


  • Track 18-1Oncogene
  • Track 18-2Pancreatic and Colorectal Cancer
  • Track 18-3Gynecologic Oncology
  • Track 18-4Melanoma and Carcinoma
  • Track 18-5Molecular & Cancer Biomarkers
  • Track 18-6Leukemia and Bone marrow Transplantation
  • Track 18-7Neoplasms
  • Track 18-8Biomedical Research
The process by which the body stops bleeding after an injury is known as hemostasis. Vasoconstriction, platelet plug formation, and activation of the coagulation cascade all take place during it, and the end consequence is the creation of a stable blood clot. The body starts to dissolve the clot and resume blood flow to the injured location once the bleeding has been halted. Disorders of clotting or bleeding can result from disturbances in the hemostatic process.
 

  • Track 19-1Hemodialysis
  • Track 19-2Thrombotic Thrombocytopenic Purpura
  • Track 19-3Hemolytic Anemia


A blood condition called thalassemia is inherited and is characterised by the body producing either an abnormal form or insufficient amounts of haemoglobin. The protein that carries oxygen in red blood cells is called haemoglobin. Anemia is brought on by the disorder's large-scale destruction of red blood cells.


  • Track 20-1Hemodialysis
  • Track 20-2Hemochromatosis
  • Track 20-3Idiopathic thrombocytopenic purpura
  • Track 20-4Malaise
  • Track 20-5Bone marrow transplantation
  • Track 20-6Blood transfusion


A range of illnesses brought on by infection with the human immunodeficiency virus are known as HIV infection and acquired immune deficiency syndrome (HIV/AIDS) (HIV). Usually, a protracted interval without symptoms comes next. As the infection worsens, it causes additional immune system interference, raising the chance of acquiring opportunistic infections, malignancies, and common illnesses like tuberculosis that seldom affect people with healthy immune systems. The term "acquired immunodeficiency syndrome" refers to these post-infection symptoms (AIDS). Unintentional weight loss is frequently correlated with this period as well.


  • Track 21-1Sexually Transmitted Diseases
  • Track 21-2Immunology and Vaccine development
  • Track 21-3Diagnosis and Treatment
  • Track 21-4Sexual Health
  • Track 21-5Clinical Research and Case Reports