SLO’s
INTRODUCTION
HISTORICAL REVIEW
EVOLUTION
CLASSIFICATION
ABOUT CLASSICAL ABO BLOOD GROUPING SYSTEM
AGGLUTINOGENS
AGGLUTININS
TYPES OF ABO BLOOD GROUPS
POPULATION DISTRIBUTION
INHERITANCE
DETERMINATION
CLINICAL IMPRTANCE
The document discusses the Rhesus blood group system, which was discovered in 1940 after testing human blood with rabbit antiserum against rhesus monkey red blood cells. It is one of the most polymorphic blood group systems, with over 45 antigens. The Rh system involves two closely linked genes, RHD and RHCE, which determine the presence of various antigens like D, C, c, E, and e. An Rh incompatibility during pregnancy can cause hemolytic disease of the newborn if a mother is Rh negative and carries an Rh positive baby.
• A blood group also called a Blood Type.
• Classification of blood is based on the presence or absence
of inherited antigenic substances on the surface of red blood
cells (RBCs).
• These antigens may be proteins, carbohydrates,
glycoproteins, or glycolipids, depending on the blood group
system.
This document summarizes the ABO blood grouping system. It describes how Karl Landsteiner discovered the A, B, and O blood groups in 1901. The system is based on the presence or absence of antigens called agglutinogens on red blood cells. People have antibodies against the agglutinogens that are not present on their own red blood cells. The genes that determine the ABO blood groups are located on chromosome 9 and are inherited according to Mendelian genetics. Blood type is determined by mixing blood cells with antisera that cause agglutination based on the antigens present.
A blood type (also called a blood group) is a classification of blood based on the presence or absence of inherited antigenic substances on the surface of red blood cells (RBCs). These antigens may be proteins, carbohydrates, glycoproteins, or glycolipids, depending on the blood group system.
This document discusses the ABO blood group system. It notes that there are over 20 known blood group systems that are genetically determined. The ABO and Rh systems are most important for blood transfusions. The ABO system involves antigens on red blood cells and corresponding antibodies in plasma. People are categorized into one of the main blood groups - A, B, AB, or O - depending on which antigens are present on their red blood cells and which antibodies are present in their plasma. The exact genetic basis and inheritance of the ABO system is also described.
The Rh blood group system is complex, with over 45 antigens. The RhD gene encodes the highly immunogenic D antigen, which is the most important antigen of the Rh system. Approximately 85% of people are RhD positive, while 15% are RhD negative. The Rh system is the second most important blood group system after ABO in transfusion medicine due to the potential for alloimmunization against the D antigen during pregnancy or transfusion. Alloimmunization to the D antigen can cause hemolytic disease of the newborn.
Karl Landsteiner discovered the ABO blood group system in 1901 by observing that mixing blood from different people sometimes caused clumping of red blood cells. He identified the A and B antigens on red blood cells and the corresponding anti-A and anti-B antibodies in plasma. Based on the presence or absence of these antigens and antibodies, he classified blood into the A, B, AB, and O groups. Landsteiner's discovery explained why blood transfusions were sometimes successful and sometimes caused fatal reactions.
The ABO blood group system was discovered in 1900 by Karl Landsteiner, who identified three main blood types: A, B, and O. The fourth type, AB, was discovered later. People have antigens on their red blood cells and corresponding antibodies in their plasma. Blood type is inherited and determines compatibility for transfusions. Type O negative blood can be donated to all recipients, while type AB positive can receive from all donors.
The document discusses the Rhesus blood group system, which was discovered in 1940 after testing human blood with rabbit antiserum against rhesus monkey red blood cells. It is one of the most polymorphic blood group systems, with over 45 antigens. The Rh system involves two closely linked genes, RHD and RHCE, which determine the presence of various antigens like D, C, c, E, and e. An Rh incompatibility during pregnancy can cause hemolytic disease of the newborn if a mother is Rh negative and carries an Rh positive baby.
• A blood group also called a Blood Type.
• Classification of blood is based on the presence or absence
of inherited antigenic substances on the surface of red blood
cells (RBCs).
• These antigens may be proteins, carbohydrates,
glycoproteins, or glycolipids, depending on the blood group
system.
This document summarizes the ABO blood grouping system. It describes how Karl Landsteiner discovered the A, B, and O blood groups in 1901. The system is based on the presence or absence of antigens called agglutinogens on red blood cells. People have antibodies against the agglutinogens that are not present on their own red blood cells. The genes that determine the ABO blood groups are located on chromosome 9 and are inherited according to Mendelian genetics. Blood type is determined by mixing blood cells with antisera that cause agglutination based on the antigens present.
A blood type (also called a blood group) is a classification of blood based on the presence or absence of inherited antigenic substances on the surface of red blood cells (RBCs). These antigens may be proteins, carbohydrates, glycoproteins, or glycolipids, depending on the blood group system.
This document discusses the ABO blood group system. It notes that there are over 20 known blood group systems that are genetically determined. The ABO and Rh systems are most important for blood transfusions. The ABO system involves antigens on red blood cells and corresponding antibodies in plasma. People are categorized into one of the main blood groups - A, B, AB, or O - depending on which antigens are present on their red blood cells and which antibodies are present in their plasma. The exact genetic basis and inheritance of the ABO system is also described.
The Rh blood group system is complex, with over 45 antigens. The RhD gene encodes the highly immunogenic D antigen, which is the most important antigen of the Rh system. Approximately 85% of people are RhD positive, while 15% are RhD negative. The Rh system is the second most important blood group system after ABO in transfusion medicine due to the potential for alloimmunization against the D antigen during pregnancy or transfusion. Alloimmunization to the D antigen can cause hemolytic disease of the newborn.
Karl Landsteiner discovered the ABO blood group system in 1901 by observing that mixing blood from different people sometimes caused clumping of red blood cells. He identified the A and B antigens on red blood cells and the corresponding anti-A and anti-B antibodies in plasma. Based on the presence or absence of these antigens and antibodies, he classified blood into the A, B, AB, and O groups. Landsteiner's discovery explained why blood transfusions were sometimes successful and sometimes caused fatal reactions.
The ABO blood group system was discovered in 1900 by Karl Landsteiner, who identified three main blood types: A, B, and O. The fourth type, AB, was discovered later. People have antigens on their red blood cells and corresponding antibodies in their plasma. Blood type is inherited and determines compatibility for transfusions. Type O negative blood can be donated to all recipients, while type AB positive can receive from all donors.
This document discusses the history and science of blood types, including the discovery of antigens and antibodies in blood and their role in determining blood compatibility. It specifically examines the rare Bombay blood type, which can receive blood from any type but can only donate to other Bombay individuals. The document stresses the importance of blood donation and registration to help those with rare blood types.
ABO blood group system was decover by Karal landsteine
which contain A, B, and o antigen on the surface of BC, WBC,s platatelet and other body tissue cells except brain cell, and anti A, antiB and Anti Ab natural occuring antibodies in plasma of B,A, and O blood group individual respectively
This document discusses blood groups and blood transfusions. It begins with an introduction to blood groups, including the ABO and Rh blood grouping systems. It describes the antigens and antibodies involved, inheritance patterns, and population distributions. It covers hemolytic disease of the newborn due to Rh incompatibility. The document also discusses blood transfusions in detail, including indications, donor and recipient selection, hazards, and storage of blood. It provides an overview of blood groups and transfusions with clinical and medical applications.
This document summarizes key aspects of blood banking. It discusses the purpose of blood banking as collecting, typing, separating, storing, and preparing blood for transfusion. It outlines the major blood group systems including ABO and Rh, which are the most immunogenic. The document compares ABO and Rh in terms of antigen location, distribution, development, and nature of antibodies. It also describes the types of blood donation and the donor selection process involving counseling, medical history, physical exam, and hemoglobin estimation. Finally, it briefly mentions types of blood bags, anticoagulants, component separation, and screening tests for diseases.
The document discusses blood groups and blood typing. It notes that the International Society of Blood Transfusion recognizes 30 major blood group systems, including the ABO and Rh systems. It specifically describes the rare Bombay blood group (hh) where individuals do not express the H antigen found in blood group O. It also defines blood typing as a lab test to determine a person's blood type and lists the worldwide and Pakistani frequencies of the main blood groups O, A, B, and AB.
The ABO blood group system was discovered in 1900 by Karl Landsteiner. He found that mixing blood samples from different people caused some to clump together, and classified human blood into three main groups - A, B, and C. In 1901 he observed that blood would only agglutinate with certain other blood groups, not its own type. This led to the modern classification of A, B, AB, and O blood groups. The fourth type, AB, which contains both A and B antigens but no antibodies, was discovered by his students in 1902. The ABO antigens are carbohydrate residues added to the H substance on red blood cells by different alleles - A adds N-acetyl glactosamine, B adds d-
This document discusses multiple blood group systems including ABO and Rh factor. It explains that the ABO system has three alleles (IA, IB, i) which determine four blood types (A, B, AB, O). The Rh system involves the D antigen, with Rh+ possessing the antigen and Rh- lacking it. Compatible blood transfusions require matching both systems to avoid hemolysis from antigen-antibody reactions. A kit test can determine blood type through agglutination reactions between cell antigens and serum antibodies.
- The Bombay blood group is an extremely rare blood type where red blood cells lack the H, A, and B antigens and plasma contains antibodies against these antigens.
- It was first discovered in Bombay, India in 1952 in about 1 in 10,000 people in Mumbai. Worldwide prevalence is about 1 in 1 million.
- People with this blood group can only receive blood from other Bombay blood group donors, as their blood will hemolyze if receiving blood from other blood groups.
- It is important for those with the Bombay blood group to register with blood banks so their rare blood can be available in emergencies.
The document discusses the ABO blood group system, including its discovery, genetics, biochemistry, antigens, antibodies, and implications for transfusion. Some key points:
- Karl Landsteiner discovered the main ABO blood groups (A, B, AB, O) in 1900. The ABO blood type is determined by alleles at a single gene locus.
- The antigens are carbohydrate structures on red blood cells. People naturally produce antibodies against antigens they lack.
- ABO typing must be accurate to avoid transfusion reactions. Discrepancies can occur due to weak subgroups, diseases, or test issues. Resolving discrepancies helps ensure patient and donor safety.
The document discusses the ABO blood group system. Some key points:
- Karl Landsteiner discovered the ABO blood group system in 1900-1901. It identifies four main blood groups: A, B, AB, and O.
- The presence or absence of A and B antigens on red blood cells determines an individual's blood group. Those without A or B antigens are group O.
- Anti-A and anti-B antibodies are naturally present in people's blood, developing after exposure to environmental antigens. These antibodies can cause hemolytic transfusion reactions if incompatible blood is transfused.
- The ABO blood groups are determined genetically based on inheritance of A, B, or O alleles. The A
This presentation discusses the ABO and Rh blood group systems. It begins by introducing Karl Landsteiner, who discovered the main blood groups in 1900. The presentation then covers the antigens and antibodies involved in blood grouping, the genetics behind blood types, and frequencies of ABO types in the US. It provides detailed explanations of the synthesis of A, B, and H antigens, including the enzymes involved. Finally, it briefly discusses the Rh system and the Rh factor.
The document summarizes key information about the rare Bombay blood group:
- The Bombay blood group lacks the H, A, and B antigens found on red blood cells, and those with this group have antibodies against these antigens in their plasma. It was first discovered in Bombay, India and is more common in some parts of India.
- Those with the Bombay blood group must receive blood from other Bombay donors, as their red blood cells will hemolyze if transfused with blood containing the H, A, or B antigens. Testing for this rare group involves reverse grouping or detection of H antibodies.
- It is important for those with the Bombay blood group to register with blood banks
This document discusses the importance of blood grouping and Landsteiner's law of blood grouping. It describes the ABO blood group system and the universal donor and recipient groups. The key blood grouping techniques of slide method and tube method are outlined. The slide method is a preliminary test while the tube method is the gold standard. The document explains the process of cell grouping (forward grouping) and serum grouping (reverse grouping) using the tube method. It also discusses grading of agglutination results and the importance of cross-matching blood prior to transfusion to avoid mismatched reactions.
The document summarizes the history and science behind blood grouping and the ABO blood group system. It describes how Karl Landsteiner discovered the major ABO blood groups in 1901. It explains the antigens and antibodies present in each blood group according to Landsteiner's rule. The genetics and biochemistry of the ABO blood group system are covered, including how the H, A, and B antigens are synthesized on red blood cells. Common blood grouping techniques like forward and reverse grouping are also summarized.
how to select a healthy donor & care of donor .A healthy donor is one of the most vital part of transfusion medicine for safe transfusion of blood & blood product
The document discusses human blood groups and the Rhesus (Rh) factor. It describes the major blood group systems, including ABO and Rh, which are most important for transfusions. The ABO system includes four blood types - A, B, AB, and O - based on the antigens on red blood cells and antibodies in plasma. The Rh system involves Rh+ and Rh- blood based on the presence or absence of Rh antigens. Incompatibility between blood groups can cause dangerous clumping of red blood cells during transfusions.
Forward and reverse grouping by Negash AlaminNegash Alamin
This document describes the forward and reverse blood grouping method used to determine a patient's blood type. The method involves separating a patient's blood into plasma and red blood cell components, mixing them in test tubes with known antibodies and blood cells, and observing for agglutination to identify reactions. If agglutination occurs, the corresponding antibody has detected the patient's blood type antigen. This method allows determining a patient's ABO blood group but not other minor blood types. It is routinely used in medical labs to identify a patient's blood type for transfusion compatibility testing.
This presentation aims to help medicine undergraduates and post graduates in the department of Pathology and Department of transfusion medicine for better understanding of various blood grouping systems, sub groups, RBC antigens and corresponding antibodies. It also covers the practical aspect of blood grouping and cross matching.
Pre-transfusion tests are performed to ensure blood compatibility and safety. These include determining the recipient's blood group and Rh type, screening the recipient's serum for antibodies, and performing a cross-match test between the recipient's serum and donor red blood cells to detect any agglutination. Additional safety tests are done on donor blood to identify infections like HIV, hepatitis B and C, and syphilis. Together these tests help select immunologically compatible blood to minimize adverse transfusion reactions in recipients.
This document outlines the components of blood and different blood grouping systems, including ABO and Rh blood typing. It discusses how Karl Landsteiner discovered human blood groups in 1901, allowing safer blood transfusions. The document describes the antigens and antibodies that determine blood type, such as A, B, and Rh factors. It explains Landsteiner's law and how blood typing is performed. Certain blood types are compatible for receiving donations from other types, with O- blood being the universal donor and AB+ being the universal receiver.
Karl Landsteiner discovered the main human blood groups (A, B, AB and O) in 1901. He found that mixing blood from two individuals can cause clumping of red blood cells. This occurs due to the presence of antigens on red blood cells and corresponding antibodies in plasma. Landsteiner's discovery made blood transfusions safer by allowing blood typing. There are over 20 blood group systems but ABO and Rh (Rhesus) are most important. ABO blood groups are determined by inheritance of A, B or O alleles while Rh status depends on presence/absence of the D antigen. Compatibility between donor and recipient blood is crucial to avoid dangerous immune reactions.
This document discusses the history and science of blood types, including the discovery of antigens and antibodies in blood and their role in determining blood compatibility. It specifically examines the rare Bombay blood type, which can receive blood from any type but can only donate to other Bombay individuals. The document stresses the importance of blood donation and registration to help those with rare blood types.
ABO blood group system was decover by Karal landsteine
which contain A, B, and o antigen on the surface of BC, WBC,s platatelet and other body tissue cells except brain cell, and anti A, antiB and Anti Ab natural occuring antibodies in plasma of B,A, and O blood group individual respectively
This document discusses blood groups and blood transfusions. It begins with an introduction to blood groups, including the ABO and Rh blood grouping systems. It describes the antigens and antibodies involved, inheritance patterns, and population distributions. It covers hemolytic disease of the newborn due to Rh incompatibility. The document also discusses blood transfusions in detail, including indications, donor and recipient selection, hazards, and storage of blood. It provides an overview of blood groups and transfusions with clinical and medical applications.
This document summarizes key aspects of blood banking. It discusses the purpose of blood banking as collecting, typing, separating, storing, and preparing blood for transfusion. It outlines the major blood group systems including ABO and Rh, which are the most immunogenic. The document compares ABO and Rh in terms of antigen location, distribution, development, and nature of antibodies. It also describes the types of blood donation and the donor selection process involving counseling, medical history, physical exam, and hemoglobin estimation. Finally, it briefly mentions types of blood bags, anticoagulants, component separation, and screening tests for diseases.
The document discusses blood groups and blood typing. It notes that the International Society of Blood Transfusion recognizes 30 major blood group systems, including the ABO and Rh systems. It specifically describes the rare Bombay blood group (hh) where individuals do not express the H antigen found in blood group O. It also defines blood typing as a lab test to determine a person's blood type and lists the worldwide and Pakistani frequencies of the main blood groups O, A, B, and AB.
The ABO blood group system was discovered in 1900 by Karl Landsteiner. He found that mixing blood samples from different people caused some to clump together, and classified human blood into three main groups - A, B, and C. In 1901 he observed that blood would only agglutinate with certain other blood groups, not its own type. This led to the modern classification of A, B, AB, and O blood groups. The fourth type, AB, which contains both A and B antigens but no antibodies, was discovered by his students in 1902. The ABO antigens are carbohydrate residues added to the H substance on red blood cells by different alleles - A adds N-acetyl glactosamine, B adds d-
This document discusses multiple blood group systems including ABO and Rh factor. It explains that the ABO system has three alleles (IA, IB, i) which determine four blood types (A, B, AB, O). The Rh system involves the D antigen, with Rh+ possessing the antigen and Rh- lacking it. Compatible blood transfusions require matching both systems to avoid hemolysis from antigen-antibody reactions. A kit test can determine blood type through agglutination reactions between cell antigens and serum antibodies.
- The Bombay blood group is an extremely rare blood type where red blood cells lack the H, A, and B antigens and plasma contains antibodies against these antigens.
- It was first discovered in Bombay, India in 1952 in about 1 in 10,000 people in Mumbai. Worldwide prevalence is about 1 in 1 million.
- People with this blood group can only receive blood from other Bombay blood group donors, as their blood will hemolyze if receiving blood from other blood groups.
- It is important for those with the Bombay blood group to register with blood banks so their rare blood can be available in emergencies.
The document discusses the ABO blood group system, including its discovery, genetics, biochemistry, antigens, antibodies, and implications for transfusion. Some key points:
- Karl Landsteiner discovered the main ABO blood groups (A, B, AB, O) in 1900. The ABO blood type is determined by alleles at a single gene locus.
- The antigens are carbohydrate structures on red blood cells. People naturally produce antibodies against antigens they lack.
- ABO typing must be accurate to avoid transfusion reactions. Discrepancies can occur due to weak subgroups, diseases, or test issues. Resolving discrepancies helps ensure patient and donor safety.
The document discusses the ABO blood group system. Some key points:
- Karl Landsteiner discovered the ABO blood group system in 1900-1901. It identifies four main blood groups: A, B, AB, and O.
- The presence or absence of A and B antigens on red blood cells determines an individual's blood group. Those without A or B antigens are group O.
- Anti-A and anti-B antibodies are naturally present in people's blood, developing after exposure to environmental antigens. These antibodies can cause hemolytic transfusion reactions if incompatible blood is transfused.
- The ABO blood groups are determined genetically based on inheritance of A, B, or O alleles. The A
This presentation discusses the ABO and Rh blood group systems. It begins by introducing Karl Landsteiner, who discovered the main blood groups in 1900. The presentation then covers the antigens and antibodies involved in blood grouping, the genetics behind blood types, and frequencies of ABO types in the US. It provides detailed explanations of the synthesis of A, B, and H antigens, including the enzymes involved. Finally, it briefly discusses the Rh system and the Rh factor.
The document summarizes key information about the rare Bombay blood group:
- The Bombay blood group lacks the H, A, and B antigens found on red blood cells, and those with this group have antibodies against these antigens in their plasma. It was first discovered in Bombay, India and is more common in some parts of India.
- Those with the Bombay blood group must receive blood from other Bombay donors, as their red blood cells will hemolyze if transfused with blood containing the H, A, or B antigens. Testing for this rare group involves reverse grouping or detection of H antibodies.
- It is important for those with the Bombay blood group to register with blood banks
This document discusses the importance of blood grouping and Landsteiner's law of blood grouping. It describes the ABO blood group system and the universal donor and recipient groups. The key blood grouping techniques of slide method and tube method are outlined. The slide method is a preliminary test while the tube method is the gold standard. The document explains the process of cell grouping (forward grouping) and serum grouping (reverse grouping) using the tube method. It also discusses grading of agglutination results and the importance of cross-matching blood prior to transfusion to avoid mismatched reactions.
The document summarizes the history and science behind blood grouping and the ABO blood group system. It describes how Karl Landsteiner discovered the major ABO blood groups in 1901. It explains the antigens and antibodies present in each blood group according to Landsteiner's rule. The genetics and biochemistry of the ABO blood group system are covered, including how the H, A, and B antigens are synthesized on red blood cells. Common blood grouping techniques like forward and reverse grouping are also summarized.
how to select a healthy donor & care of donor .A healthy donor is one of the most vital part of transfusion medicine for safe transfusion of blood & blood product
The document discusses human blood groups and the Rhesus (Rh) factor. It describes the major blood group systems, including ABO and Rh, which are most important for transfusions. The ABO system includes four blood types - A, B, AB, and O - based on the antigens on red blood cells and antibodies in plasma. The Rh system involves Rh+ and Rh- blood based on the presence or absence of Rh antigens. Incompatibility between blood groups can cause dangerous clumping of red blood cells during transfusions.
Forward and reverse grouping by Negash AlaminNegash Alamin
This document describes the forward and reverse blood grouping method used to determine a patient's blood type. The method involves separating a patient's blood into plasma and red blood cell components, mixing them in test tubes with known antibodies and blood cells, and observing for agglutination to identify reactions. If agglutination occurs, the corresponding antibody has detected the patient's blood type antigen. This method allows determining a patient's ABO blood group but not other minor blood types. It is routinely used in medical labs to identify a patient's blood type for transfusion compatibility testing.
This presentation aims to help medicine undergraduates and post graduates in the department of Pathology and Department of transfusion medicine for better understanding of various blood grouping systems, sub groups, RBC antigens and corresponding antibodies. It also covers the practical aspect of blood grouping and cross matching.
Pre-transfusion tests are performed to ensure blood compatibility and safety. These include determining the recipient's blood group and Rh type, screening the recipient's serum for antibodies, and performing a cross-match test between the recipient's serum and donor red blood cells to detect any agglutination. Additional safety tests are done on donor blood to identify infections like HIV, hepatitis B and C, and syphilis. Together these tests help select immunologically compatible blood to minimize adverse transfusion reactions in recipients.
This document outlines the components of blood and different blood grouping systems, including ABO and Rh blood typing. It discusses how Karl Landsteiner discovered human blood groups in 1901, allowing safer blood transfusions. The document describes the antigens and antibodies that determine blood type, such as A, B, and Rh factors. It explains Landsteiner's law and how blood typing is performed. Certain blood types are compatible for receiving donations from other types, with O- blood being the universal donor and AB+ being the universal receiver.
Karl Landsteiner discovered the main human blood groups (A, B, AB and O) in 1901. He found that mixing blood from two individuals can cause clumping of red blood cells. This occurs due to the presence of antigens on red blood cells and corresponding antibodies in plasma. Landsteiner's discovery made blood transfusions safer by allowing blood typing. There are over 20 blood group systems but ABO and Rh (Rhesus) are most important. ABO blood groups are determined by inheritance of A, B or O alleles while Rh status depends on presence/absence of the D antigen. Compatibility between donor and recipient blood is crucial to avoid dangerous immune reactions.
Karl Landsteiner discovered the main human blood group systems in 1901 which allowed safer blood transfusions. He found that mixing blood from two individuals can cause clumping if they have incompatible blood types due to antigens and antibodies. There are four main blood types - A, B, AB and O based on the presence or absence of A and B antigens on red blood cells and the corresponding antibodies in plasma. The Rh system further divides blood into Rh+ and Rh- based on the presence of the Rh antigen. Understanding blood groups is crucial to ensure compatibility during transfusions.
The document provides an overview of blood groups and blood typing systems. It discusses the history and discovery of blood groups, the ABO and Rh blood typing systems, inheritance of blood groups, clinical applications like blood transfusions and preventing hemolytic disease of the newborn. It describes the antigens and antibodies involved in blood typing, determining blood groups, population distributions of blood groups, and precautions for blood transfusions.
The ABO blood group system is one of the most important blood group systems for transfusions. It is determined by the ABO gene which has three alleles - IA, IB, and i - that encode for the A, B, and O antigens, respectively. The ABO blood types are determined by which alleles are present: IAIA or IAi produce type A blood, IBIB or IBi produce type B, IAIB produces AB, and ii produces O. The Rh system, specifically the D antigen, is the second most important blood group and sensitization to the D antigen in Rh-negative pregnant women can cause hemolytic disease of the newborn if not prevented.
There are over 30 known blood group systems that contain around 400 antigens. The most important systems for blood transfusions are ABO and Rh. The ABO system contains A, B, and H antigens. People are type A, B, AB, or O based on which antigens are present. Naturally occurring antibodies are directed against antigens not present on one's own red blood cells. The Rh system contains D and other antigens. Most people are Rh+ or Rh-. Rh incompatibility can cause hemolytic disease of the newborn.
This presentation summarizes the ABO blood group system. It defines blood groups as classifications based on antigens on red blood cells, with over 30 known human blood group systems containing over 600 antigens. The ABO system was discovered by Karl Landsteiner in 1901 and recognizes the A, B, AB, and O blood groups based on the presence or absence of A and B antigens. The characteristics of each blood group determine who can donate to and receive from whom. ABO antibodies are clinically significant as they are naturally occurring, universal, and highly reactive. Understanding blood groups is important for transfusion safety and other medical applications.
This document summarizes blood types and blood compatibility for transfusion. It discusses:
- The four main blood groups (A, B, AB, O) based on the presence or absence of antigens on red blood cells.
- The corresponding antibodies found in plasma (anti-A, anti-B) which cause agglutination during incompatible transfusions.
- Blood type O is the universal donor as it lacks antigens, while type AB is the universal receiver as it lacks antibodies.
- Compatibility for donation and receipt of blood is determined by the antigen-antibody relationship between donor and recipient blood types.
5th year (Blood bank and blood transfusion).pptxMostafaAdelAhmd
The document discusses the history and science of blood banking and transfusion. It covers early attempts at blood transfusions dating back to ancient times. Major milestones include the discovery of the ABO blood group system in 1900 and the Rh system in 1940. The document also examines blood group inheritance and genetics. It provides details on the ABO and Rh blood group systems, including antigens, antibodies, donation compatibility, and inheritance patterns.
A elaborate note on "ABO Blood Group System"
All the concept related to ABO blood group (i.e.; from basics to genetics, biochemistry & heredity) is clearly described here.
If any question your mind approach, comment bellow, your doubt will be surely cleared through my reply.
THANK YOU
The document discusses blood groups and their types. It begins with definitions of blood groups and why knowing types is important. The four main blood groups are then explained: A, B, AB, and O. The history of discovering blood groups is provided, with Karl Landsteiner first identifying the four types in 1901. Methods for determining blood group are also outlined, including the tube method. Reasons for blood transfusions and matching blood types are explained.
Blood group (population genetic and evolution) by nagendra sahuNagendrasahu6
This document provides information about different blood group types including ABO and Rh blood grouping systems. It discusses the discovery of blood groups by Karl Landsteiner who received the Nobel Prize for this work. The four main blood groups based on ABO antigens are described as well as inheritance of these antigens. The importance of matching blood types during transfusions and issues that can arise from mismatches like agglutination are explained. Rh factor and hemolytic disease in newborns due to Rh incompatibility are also summarized. The document concludes with brief information about the MNS blood grouping system.
A blood group also called a Blood Type
Classification of blood is based on the presence or absence of inherited antigenic substances on the surface of red blood cells (RBCs)
These antigens may be proteins, carbohydrates, glycoproteins, or glycolipids, depending on the blood group system.
The ABO blood group system is the most important blood type system (or blood group system) in human blood transfusion.
ABO blood types are also present in some other animals for example rodents and apes such as chimpanzees, bonobos and gorillas.
Different blood groups and their their significances..Amjad Afridi
The document discusses different blood group systems and their significance. It covers the discovery of the ABO blood group system by Karl Landsteiner in 1901. The major blood group systems are ABO and Rh, while minor systems include Lewis, Duffy, Kidd, Kell, Lutheran. The ABO system categorizes blood as A, B, AB, or O based on antigens on red blood cells. Compatibility in transfusions depends on the absence of antigens and presence of antibodies. People with type O blood are universal donors as they lack A and B antigens, while those with type AB blood are universal recipients.
Karl Landsteiner discovered the main human blood groups (A, B, AB, and O) in 1901. This discovery allowed safer blood transfusions by preventing fatal reactions between incompatible blood groups. The presence or absence of antigens (proteins) and antibodies on red blood cells and in plasma determines a person's blood group. The ABO and Rh blood group systems are most important for transfusions. A person can only receive blood from a donor with compatible or identical blood groups to prevent dangerous clumping of red blood cells.
The document discusses blood grouping methodology and focuses on the ABO and Rh blood group systems. It provides details on:
- The ABO blood group system is the most clinically important and is determined by the presence or absence of A and B antigens on red blood cells. The Rh system involves the D antigen.
- Karl Landsteiner discovered the ABO system in 1901 and was awarded the Nobel Prize for his work. Inheritance of blood groups follows genetic patterns.
- Common techniques for blood grouping include slide tests, tube tests, microplates, and gel cards. Proper sample collection and testing procedures must be followed.
- Understanding blood groups is essential for safe blood transfusions and preventing issues like hemolytic
The document summarizes key information about blood groups and genetics. It discusses how blood type is determined by genes inherited from parents, which cause proteins called agglutinogens on red blood cells. The main blood group systems - ABO and Rh - are described. Landsteiner's laws explain the relationship between agglutinogens and agglutinins in different blood types. Compatibility between donor and recipient blood depends on preventing agglutination during transfusion. Complications can be avoided through proper cross-matching and screening of donor blood.
Optics of Vision II - photochemistry dyp.pptxPandian M
1) The document discusses the structure and function of photoreceptor cells (rods and cones) in the retina and the biochemical process of vision, including the roles of rhodopsin and retinal isomerization.
2) It also explains the visual cycle and how activation of rhodopsin causes hyperpolarization in the rod cell, leading to a receptor potential.
3) Finally, it covers common errors of refraction like myopia, hyperopia, astigmatism, and presbyopia as well as visual field defects that can result from lesions along the visual pathway from the retina to the visual cortex.
The thalamus is located in the center of the cerebral hemispheres. It receives sensory input from various areas and projects to different cortical regions. The thalamus and cortex work as a single functional unit, with the thalamus integrating inputs and the cortex performing higher-level processing.
Anatomically, the thalamus is divided into anterior, lateral, and medial groups of nuclei. The lateral group contains sensory relay nuclei that project to sensory cortices. Association nuclei in the medial and dorsal groups integrate sensory and limbic inputs and project to association cortices. Nonspecific nuclei in the intralaminar and midline regions are involved in arousal, emotions, and alertness.
Damage to the
Pulmonary surfactant is produced by type II alveolar cells and acts to reduce surface tension in the lungs. It is composed primarily of phospholipids including dipalmitoyl phosphatidylcholine and surfactant proteins. Surfactant functions to prevent alveolar collapse during exhalation by reducing surface tension and to maintain uniform alveolar size. Disruption of surfactant production can lead to respiratory distress syndrome in newborns and adults with lung injury.
The document discusses key concepts related to patients and illness. It defines a patient as someone suffering from an illness and receiving medical treatment. It describes acute illnesses as short-term and severe, while chronic illnesses persist for over 6 months and may cause disability. The stages of illness behavior are discussed, from initially experiencing symptoms, to assuming the sick role and seeking medical care, becoming dependent on treatment, and recovering. Emotional responses like fear and anxiety are also reviewed.
This document discusses white blood cell formation and regulation. It begins by explaining that leukopoiesis (white blood cell formation) is mainly regulated by cytokines like colony stimulating factors, interleukins, and tumor necrosis factors which are produced by tissues like T lymphocytes, monocytes, fibroblasts and organs like the liver and kidneys. It then goes on to describe various conditions that can cause changes in different white blood cell counts, including physiological and pathological causes of neutrophilia, neutropenia, eosinophilia, basophilia, lymphocytosis, lymphocytopenia, monocytosis and monocytopenia. Examples of diseases or situations associated with increases or decreases in specific white blood cell types are provided. The document concludes by listing
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Cardiac muscle has unique properties that allow the heart to function as a syncytium.
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2) The heart has specialized pacemaker cells in the sinoatrial node that generate action potentials spontaneously due to unstable membrane potentials and funny channels.
3) Cardiac action potentials have a plateau phase due to calcium influx through L-type calcium channels, allowing the heart to contract forcefully for over 200ms.
The document discusses renal tubular reabsorption and secretion. It covers:
1. The proximal tubule reabsorbs about 65% of filtered sodium, chloride, bicarbonate, potassium, and essentially all filtered glucose and amino acids. It also secretes organic acids, bases, and hydrogen ions.
2. In the loop of Henle, the descending limb reabsorbs water by passive diffusion. The thick ascending limb actively reabsorbs sodium, chloride, and potassium.
3. The distal tubules and collecting ducts reabsorb approximately 7% of filtered NaCl and 8-17% of water. They secrete potassium and hydrogen ions. The medullary collecting duct is perme
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2. It describes the anatomy and innervation of the urinary bladder, as well as the mechanism of micturition and how micturition is controlled.
3. Various bladder dysfunctions that can occur due to lesions at different levels of the neuraxis are also discussed.
The countercurrent mechanism involves the loops of Henle and vasa recta working together to create and maintain an osmotic gradient in the renal medulla. The loops of Henle function as countercurrent multipliers, actively transporting ions from the thick ascending limb to increase the osmolarity of the interstitial fluid. The vasa recta parallel the loops of Henle and function as countercurrent exchangers, rapidly exchanging fluids between ascending and descending limbs to minimize washing out solutes and preserve the osmotic gradient as blood flows through the medulla. This countercurrent system allows urine to be concentrated as water is reabsorbed along the nephron according to the osmotic gradient in the
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COMPOSITION
BLOOD CELLS
PLASMA
SERUM
FUNCTIONS
NUTRITIVE FUNCTION
RESPIRATORY FUNCTION
EXCRETORY FUNCTION
TRANSPORT OF HORMONES AND ENZYMES
REGULATION OF WATER BALANCE
REGULATION OF ACID-BASE BALANCE
REGULATION OF BODY TEMPERATURE
STORAGE FUNCTION
DEFENSIVE FUNCTION
Blood is a connective tissue composed of plasma and cellular elements. Plasma is 55% of blood and contains water, proteins, nutrients, gases, and electrolytes. Cellular elements include red blood cells, white blood cells, and platelets. Red blood cells transport oxygen and carbon dioxide. White blood cells help fight infection. Platelets help with blood clotting. Blood has many functions including nutrient transport, waste removal, temperature regulation, hormone transport, and immune defense. Anemia is a decrease in red blood cells or hemoglobin and can be caused by blood loss, increased cell destruction, or decreased cell production.
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Dr. Pandian M describes the procedure for performing a platelet count. Platelets serve important hemostatic functions and their normal range is 1.5-4 lakhs/cumm. The procedure involves mixing blood with a diluting fluid in a Neubauer chamber, then counting platelets in grid squares under a microscope. For the sample, 40 platelets were counted in 1/50 mm3, indicating a platelet count of 2 lakhs/mm3 of blood, within the normal range. Abnormally high or low platelet counts can occur due to various bone marrow and other disorders.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
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Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
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2. SLO’s
INTRODUCTION
HISTORICAL REVIEW
EVOLUTION
CLASSIFICATION
ABOUT CLASSICAL ABO BLOOD GROUPING SYSTEM
o AGGLUTINOGENS
o AGGLUTININS
o TYPES OF ABO BLOOD GROUPS
o POPULATION DISTRIBUTION
o INHERITANCE
o DETERMINATION
o CLINICAL IMPRTANCE
3. INTRODUCTION
BLOOD GROUP : An inherited antigen on
surface of RBCs determining blood group
Series of blood types constitute the blood
group system
5. CLASSIFICATION
More than 50 genetically determined blood group
systems
2 blood group systems were discovered by
LANDSTEINER i.e. ABO system and RH system
LEWIS blood group system was discovered by
MR.LEWIS,presence of which causes some
complications such as retarded growth, sometimes
causes transfusion reactions also and this blood group
is more prone to H-pylori infection.
Rh,MNS,P,Duffy,Luis, Kell,Kidd,Lutheran,Bombay
Blood Group
6. RBC’s membranes
there are various
antigens called as
agglutinogens.
This antigens decide
the blood groups of
person.
7. History & Evolution
Back in early days, there were only blood type ‘O’
people i.e. the surfaces of their RBCs had neither A nor
B antigens
Around 20,000 B.C.,some mutation occurred, some
people began to have blood type A and developed A
antigen on the surface of their RBCs..it was observed in
CENTRAL EUROPE as well as SCANDANAVIA
Next change was observed around 10,000 B.C.when
some people developed type B antigen on their blood
cells this change occurs in ASIA and JAPAN and
biologists were not sure what encouraged this change to
take place.
8. History & Evolution
It was not till 1500s that A and B GROUPS began to mix
as travel becomes more common..this formed AB blood
type, which is now more common in NORTHERN INDIA.
It was only in 1909 that doctors finally figured out what
caused some blood transfusions to work and others to
fail!!!!!!!
9. Types Of Blood Groups
Depending upon the type
of agglutinogen present
there are 4 blood groups-
A,B,AB and O.
The antigen-H is common
in all the blood groups.
10. ABO System/ ABH System
ABO system is also
based on the
aggutinogens present on
the RBCs.
The ABO blood group
antigens are all
membrane glycolipids.
It mainly contains 3
agglutinogens A,B and
H.
12. Landsteiner’s Law
In 1900 , Karl Landsteiner framed this law which is
divided into 2 major components-
1) If an agglutinogen is present in the RBCs of
individual, the corresponding agglutinin must be
absent from the plasma.(for ABO & Rh systems)
2)If the agglutinogen is absent in the individual
RBCs, the corresponding agglutinin must be
present in plasma.(for ABO system)
13.
14. AGGLUTINOGENS
Antigens type A and B are present on cell
membrane of RBCs in large proportion, called
as AGGLUTINOGENS
They determine the type of blood group
Agglutinogens A and B first appeared in 6th
week of foetal life..their concentration
increases progressively during puberty and
adolescence.
15. AGGLUTININS
GAMMA GLOBULINS, produced by same
cells that produce anti bodies to any other
antigens
Mostly are IgM and develops in PLASMA
At birth, quantity of agglutinin is almost zero..
At 2-8 months, agglutinin formation starts.
17. TYPES OF ABO BLOOD GROUPS
GROUP ANTIGEN IN
RBCs
ANTIBODY IN
SERUM
A A ANTI-B
B B ANTI-A
AB A and B NO ANTIBODY
O H BOTH ANTI-A
& ANTI-B
18.
19. INHERITANCE OF BLOOD
GROUPS
Classical blood groups depend on 3
genes:A,B,O
Each persons blood group is determined by
two genes which he receives from each parent
However, child’s blood may not be set in its
true ABO type until as late as one year after
birth
22. 1)Blood Typing or grouping.
2)Certain Blood Studies
O’ blood group individual are more prone to
duodenal ulcer(peptic ulcer)
‘A’ blood group individual are more prone to
carcinoma of stomach ,pancreas and
salivary gland .
23. 3)Paternity test –To prove person is not father of child.
If child’s blood group is AB father’s blood group
cannot be O
4)Forensic medicine-DNA Finger printing –A drop of
blood is sufficient to identify criminal.
24. Universal Donor
O Rh Negative is universal donor.
AB Rh positive is universal receipent.
25. Summary
‘Classical ABO Blood Group System
4 blood groups- A,B,AB and O.
Inherited as Mendelian Codominant.
AB is universal receipent and O is
universal donor.
26. Bombay Blood Group
This rare blood group was first detected in
Mumbai (Bombay) India, a few decades back,
consisting of people who did not have any of
the standard blood groupings: A, AB, B or O.,
and called the Bombay Blood Group.
The Bombay Blood Group, known as Oh,
occurs when the person has a homozygous
state of a rare recessive gene. It can be
detected either by reverse grouping or Serum
grouping of the blood.
27. The Bombay Blood Group is incompatible with
all A, B and O donors and is considered the
rarest known blood type, except in parts of
India where it occurs in 1 out of 7,600 people.
The Bombay blood group is missing an
antigen present on cells of the ABO group,
the H antigen. The H antigen is a
carbohydrate known as fucose.
28. MNS system:MNS blood group reacts
with ANTI –M,ANTI-N,ANTI-S
oIt helps in paternity disputes. From this
blood group testing we can show that the
suspected person could not possibly have
been the father.
Other systems include:AUBERGER
GROUP,BOMBAY GROUP,DIEGO
GROUP,DUFFY GROUP,KIDD
GROUP,SULTER Xg GROUP
29. References
Text book of Medical Physiology
Guyton & Hall
Human Physiology
Vander
Text book of Medical Physiology
Indukurana
Principles of Anatomy and Physiology
Totora
Net source