Rare Blood 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.

 

  • Diagnosis and Management of Rare Anemias
  • Rare Coagulation Factor Deficiencies: Diagnosis and Treatment
  • Emerging Therapies for Paroxysmal Nocturnal Hemoglobinuria (PNH)

Related Conference of Rare Blood Disorders

June 20-21, 2024

20th Global Summit on Hematology and Infectious Diseases

Dublin, Ireland

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