Hemophilia
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Hemophilia is a disease where the blood is too thin and cannot clot properly, causing prolonged bleeding from cuts or injuries. It is inherited through family lines and is more common in males. Symptoms include bleeding that does not stop as it normally would. Diagnosis involves testing by a doctor if bleeding issues are noticed or if there is a family history of hemophilia. It affects around 18,000 people in the United States and is treated by replacing the missing clotting factors through intravenous injections.
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Hemophilia
Hemophilia is a hereditary bleeding disorder caused by a deficiency of specific clotting factors, which prevents normal blood clotting. The two main types are hemophilia A caused by a factor VIII deficiency and hemophilia B caused by a factor IX deficiency. Symptoms include excessive bleeding, easy bruising, and bleeding into joints. It is usually passed from mother to son and is treated through replacement of the deficient clotting factor. Nursing care focuses on prevention of injury, control of bleeding episodes, and prevention of joint damage.
Hemophilia
Hemophilia is a rare inherited blood clotting disorder caused by deficient blood proteins. It is passed down from mother to son through genes on the X chromosome. Symptoms include prolonged bleeding from cuts or wounds and internal bleeding in joints that can lead to arthritis if untreated. Physicians test for hemophilia by ruling out other disorders and determining which clotting factor is deficient. About 1 in 4,000 males have the disorder. Treatment involves regularly injecting purified clotting factors to prevent or stop bleeding episodes.
Progeria , by Lucia
Progeria is a rare genetic disorder that causes children to age rapidly, experiencing problems usually seen in the elderly like heart disease, stiffness of joints, and loss of hair and body fat. It affects around 50 children worldwide. Children with Progeria appear to have the appearance of an elderly person and most die of heart attacks or strokes at an average age of 13 years old. There is no cure for Progeria but treatments can help manage symptoms and delay the effects of aging.
Hemoglobin and Level of Hemoglobin Required in the Body
Hemoglobin is a protein present in the red blood cells. The red color pigmentation of the blood is because of hemoglobin. Hemoglobin is the primary oxygen-carrying protein that circulates throughout the blood.
Sickle cell anaemia
Haemoglobinopathies are genetically inherited blood disorders caused by abnormalities in the haemoglobin protein. The most common types are sickle cell anaemia and thalassaemia. Sickle cell anaemia results from abnormal haemoglobin HbS which causes red blood cells to become sickle shaped and destroy easily. Thalassaemia involves absent or reduced globin chains leading to anaemia. Management involves treating crises, infections, and anemia with blood transfusions and medications. Pregnancy requires special care due to risks of complications.
Hemophilia
Hemophilia is an inherited bleeding disorder caused by deficient or defective clotting factors. There are three main types - Hemophilia A caused by Factor VIII deficiency, Hemophilia B caused by Factor IX deficiency, and Hemophilia C caused by Factor XI deficiency. Hemophilia A accounts for about 98% of cases and is X-linked recessive inherited. Symptoms range from easy bruising to spontaneous internal bleeding. Diagnosis involves blood tests of clotting factors and family history. Treatment focuses on replacement of missing clotting factors through infusion or preventing bleeding through antifibrinolytic drugs.
Bariatric Vitamin Deficiency - Don't Fall Victim
Some common symptoms of anemia include shortness of breath, fatigue, paleness, dizziness, and fainting. More severe anemia can cause chest pain, headaches, and difficulty walking. Megaloblastic anemia is often caused by vitamin B12 or folate deficiencies and can result from conditions like alcoholism that inhibit nutrient absorption. Herbal teas made from ingredients like red raspberry leaves and lady's mantle can help treat mild anemia symptoms before and during menstruation.
Marie nzala sickle cell disease
Sickle cell anemia is a genetic blood disorder caused by abnormal hemoglobin in red blood cells. It was first discovered in 1910 by Dr. James Herrick in a patient presenting with anemia and pain episodes. The genetic mutation causes hemoglobin to form stiff, sickle shapes that can block blood vessels. It is inherited in an autosomal recessive pattern, requiring both parents to carry the gene. Those most commonly affected are those with ancestry from sub-Saharan Africa, South America, Central America, Saudi Arabia, India, and Mediterranean countries. Symptoms include anemia crises, pain episodes, infections, and organ damage. Treatment focuses on pain management, antibiotics, hydration, folic acid, and hydroxy
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Hemophilia
Hemophilia is a hereditary bleeding disorder caused by a deficiency of specific clotting factors, which prevents normal blood clotting. The two main types are hemophilia A caused by a factor VIII deficiency and hemophilia B caused by a factor IX deficiency. Symptoms include excessive bleeding, easy bruising, and bleeding into joints. It is usually passed from mother to son and is treated through replacement of the deficient clotting factor. Nursing care focuses on prevention of injury, control of bleeding episodes, and prevention of joint damage.
Hemophilia
Hemophilia is a rare inherited blood clotting disorder caused by deficient blood proteins. It is passed down from mother to son through genes on the X chromosome. Symptoms include prolonged bleeding from cuts or wounds and internal bleeding in joints that can lead to arthritis if untreated. Physicians test for hemophilia by ruling out other disorders and determining which clotting factor is deficient. About 1 in 4,000 males have the disorder. Treatment involves regularly injecting purified clotting factors to prevent or stop bleeding episodes.
Progeria , by Lucia
Progeria is a rare genetic disorder that causes children to age rapidly, experiencing problems usually seen in the elderly like heart disease, stiffness of joints, and loss of hair and body fat. It affects around 50 children worldwide. Children with Progeria appear to have the appearance of an elderly person and most die of heart attacks or strokes at an average age of 13 years old. There is no cure for Progeria but treatments can help manage symptoms and delay the effects of aging.
Hemoglobin and Level of Hemoglobin Required in the Body
Hemoglobin is a protein present in the red blood cells. The red color pigmentation of the blood is because of hemoglobin. Hemoglobin is the primary oxygen-carrying protein that circulates throughout the blood.
Sickle cell anaemia
Haemoglobinopathies are genetically inherited blood disorders caused by abnormalities in the haemoglobin protein. The most common types are sickle cell anaemia and thalassaemia. Sickle cell anaemia results from abnormal haemoglobin HbS which causes red blood cells to become sickle shaped and destroy easily. Thalassaemia involves absent or reduced globin chains leading to anaemia. Management involves treating crises, infections, and anemia with blood transfusions and medications. Pregnancy requires special care due to risks of complications.
Hemophilia
Hemophilia is an inherited bleeding disorder caused by deficient or defective clotting factors. There are three main types - Hemophilia A caused by Factor VIII deficiency, Hemophilia B caused by Factor IX deficiency, and Hemophilia C caused by Factor XI deficiency. Hemophilia A accounts for about 98% of cases and is X-linked recessive inherited. Symptoms range from easy bruising to spontaneous internal bleeding. Diagnosis involves blood tests of clotting factors and family history. Treatment focuses on replacement of missing clotting factors through infusion or preventing bleeding through antifibrinolytic drugs.
Bariatric Vitamin Deficiency - Don't Fall Victim
Some common symptoms of anemia include shortness of breath, fatigue, paleness, dizziness, and fainting. More severe anemia can cause chest pain, headaches, and difficulty walking. Megaloblastic anemia is often caused by vitamin B12 or folate deficiencies and can result from conditions like alcoholism that inhibit nutrient absorption. Herbal teas made from ingredients like red raspberry leaves and lady's mantle can help treat mild anemia symptoms before and during menstruation.
Marie nzala sickle cell disease
Sickle cell anemia is a genetic blood disorder caused by abnormal hemoglobin in red blood cells. It was first discovered in 1910 by Dr. James Herrick in a patient presenting with anemia and pain episodes. The genetic mutation causes hemoglobin to form stiff, sickle shapes that can block blood vessels. It is inherited in an autosomal recessive pattern, requiring both parents to carry the gene. Those most commonly affected are those with ancestry from sub-Saharan Africa, South America, Central America, Saudi Arabia, India, and Mediterranean countries. Symptoms include anemia crises, pain episodes, infections, and organ damage. Treatment focuses on pain management, antibiotics, hydration, folic acid, and hydroxy
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This document discusses thalassemia, an inherited blood disorder caused by missing or abnormal genes that affect hemoglobin production. It describes alpha and beta thalassemia specifically. Alpha thalassemia results from changes in genes for the alpha globin component and is most common in areas historically affected by malaria. Beta thalassemia is caused by a deficiency in beta globin production inherited in an autosomal recessive pattern. Symptoms range from mild anemia to severe anemia and organ enlargement. Treatment involves regular blood transfusions, iron chelation drugs, and sometimes splenectomy or bone marrow transplant.
Hemophila pp
Hemophilia is a genetic bleeding disorder caused by mutations on the F8 gene located on the X chromosome. People with hemophilia experience prolonged bleeding from minor injuries due to a lack of clotting factor VIII or IX in their blood. Treatment involves replacement therapy through frequent injections of clotting factor concentrates. While treatment allows people with hemophilia to live normal lives, risks include developing antibodies against the clotting factor and bleeding complications. Researchers are studying gene therapy as a potential cure by correcting the defective genes that cause hemophilia.
Genetic Disorders
Genetic disorders may be Mendelian and Chromosomal disorders.
example- Haemophilia, Sickle cell anemia, THalessemia, Colour Blindness, Phenylketonuria, Cystic fibrosis, Turner Syndromes etc
SICKLE CELL ANAEMIA IN PREGNANCY FOR MBBS UNDER GRADUATES OBG
Sickle cell anemia is caused by a point mutation that substitutes valine for glutamic acid in the beta globin chain of hemoglobin. This causes red blood cells to sickle under conditions of hypoxia, acidosis, cold, or dehydration. Sickling leads to hemolytic anemia and vaso-occlusive crises that can damage organs. Pregnancy further complicates sickle cell anemia by increasing risks of painful sickle cell crises, preeclampsia, and fetal growth restriction. Management involves preconception counseling, frequent monitoring during pregnancy for complications, and aggressive treatment of crises and infections to support a healthy pregnancy outcome.
Sickle cell anemia
Sickle Cell disease: is a genetic disorder that affects erythrocytes (RBC) causing them
to become sickle or crescent shaped.
The effects of this condition due to an abnormality of the hemoglobin molecules found
in erythrocytes.
Sickle cell anemia is a serious disease in which the body makes sickle-shaped red blood
cells. “Sickle-shaped” means that the red blood cells are shaped like a "C."
Normal red blood cells are disc-shaped and look like doughnuts without holes in the
center. They move easily through your blood vessels. Red blood cells contain the
protein hemoglobin. This iron-rich protein gives blood its red color and carries oxygen
from the lungs to the rest of the body.
Sickle cell Anemia is known as being a fatal hereditary form of anemia, it is recognized
by its abnormal red blood cells having a crescent shape due to the effect of hemoglobin
S found in the cells.
Thalassemia, blood,disorder,hemoglobin,red .cells
Thalassemia is a genetic blood disorder where the body produces unhealthy red blood cells and less hemoglobin. It is caused by mutations in the genes that make hemoglobin. There are two main types - alpha thalassemia and beta thalassemia. Symptoms include fatigue, weakness, and pale skin due to anemia. While there is no cure, treatment focuses on blood transfusions and chelation therapy to manage excess iron in the blood from the transfusions.
Sickle cell disease sandip
1. Sickle cell disease is an inherited blood disorder that affects hemoglobin and causes red blood cells to take on a sickle, or crescent, shape.
2. The prevalence of sickle cell disease varies by ethnicity, with the highest rates seen in African Americans at about 1 in 375 individuals.
3. Complications of sickle cell disease include anemia, infections, acute pain episodes, stroke, and damage to organs like the lungs, kidneys, spleen, and liver over time if not properly managed.
Anemia
Anemia is defined as a reduction in red blood cells or hemoglobin. It has many potential causes including blood loss, decreased bone marrow production, and genetic disorders. Symptoms include fatigue, palpitations, and shortness of breath. Diagnosis involves a complete blood count, peripheral smear, and identifying the underlying cause through history, examination, and additional testing. Treatment depends on the specific cause but may include iron supplementation, B12/folate, blood transfusions, or immunosuppressive drugs.
sickle cell anemia
Sickle cell anemia is an inherited form of anemia where red blood cells become rigid and shaped like sickles or crescents, due to a genetic mutation causing abnormal hemoglobin. Symptoms usually appear after 4 months and include abdominal pain, bone pain, breathing difficulties, fatigue, fever, and jaundice. Treatment focuses on managing symptoms, limiting crises, and taking folic acid supplements to support red blood cell production.
Klinefelter syndrome
Klinefelter syndrome is a genetic condition where males are born with an extra X chromosome, resulting in XXY. It can cause smaller testes and lower testosterone production, leading to reduced muscle and facial/body hair and enlarged breasts. It was first identified in 1942 in males with these symptoms. Testing hormone levels and chromosomes can diagnose it, and treatments aim to replace testosterone and address specific symptoms.
Oligospermia - Indira IVF
The point at which the male accomplice has low sperm count or under 15 million sperm for each ml in discharge due to Oligospermia, this impacts the male regenerative framework and can not prepare an egg. Accordingly female accomplice unfit to imagine pregnancy because of less sperm tally. Visit Indira IVF for appropriate direction to dispose of male infertility.
Hemophilia
This document provides information about hemophilia, including:
- Hemophilia is an inherited bleeding disorder caused by deficiencies in specific clotting factors like VIII or IX.
- There are three main types - A, B, and C - determined by which clotting factor is deficient.
- It is passed from parents to children via genes on the X chromosome.
- Symptoms include bruising and bleeding, especially into joints or muscles. Treatment aims to prevent bleeding complications through blood transfusions or replacement of the deficient clotting factor.
Fabry Disease Ppt.Cyrus & Jukie
Fabry disease is a rare genetic disorder caused by deficient activity of the enzyme alpha-galactosidase A. This enzyme breakdown lipids in the body. Its deficiency leads to a buildup of lipids in blood vessels, kidneys, and other organs. Symptoms include skin lesions, pain, kidney failure, and increased risk of heart disease. Treatment involves enzyme replacement therapy via intravenous infusion to help break down the buildup of lipids. However, this treatment does not cure the condition but only manages symptoms.
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Thalassemia
Thalassemia is a genetic blood disorder characterized by defective or reduced hemoglobin. There are two main types: alpha thalassemia affects alpha globin chain production and beta thalassemia affects beta globin chain production. Symptoms range from mild anemia to severe anemia requiring regular blood transfusions depending on which genes are affected. Treatment involves lifelong blood transfusions combined with iron chelation therapy to prevent iron overload, and potentially splenectomy or bone marrow transplant.
Alpha thalassemia
presented by HAFIZ M WASEEM
university of education LAHORE Pakistan
i am from mailsi vehari and studied in lahore
Sickle Cell Anemia
Sickle cell Anemia is known as being a fatal hereditary form of anemia, it is recognized by its abnormal red blood cells having a crescent shape due to the effect of hemoglobin S found in the cells.
Post, Blog and Get Paid,
http://cashpaydaily.net
In the United States approximately 1 in every 375 African Americans are born with Sickle Cell Disease each year.
Sickle Cell Anemia is most common among people whose ancestors came from sub-Saharan Africa; Spanish-speaking regions in the Western Hemisphere (South America, the Caribbean, and Central America); Saudi Arabia; India; and Mediterranean countries such as Turkey, Greece, and Italy.
Sickle Cell Anemia occurs more often among people from parts of the world where Malaria is common.
Interesting Fact: People who have the sickle cell trait, (gene) are less likely to have severe forms of Malaria.
Home Base Business Opportunities
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A complete 8-Step 'Money Getting' Formula ($297 Value) In this High-Value Video Training Series, I'll learn the most effective ways to build a successful online business and the Core 'Must Have' principals to Effective Entrepreneurship in today’s market. These videos outline your BIGGEST money making principals all in one place Watch Video Here http://freedomofsuccess.com
anemia and thalassemia genetic bases ,the molecular defects and pathophysiol...
anemia and thalassemia genetic bases ,the molecular defects and pathophysiol...imam univarsity , college of medicine .
1• Define anemia and it's genetic bases.2• Describe thalassemia and it's genetic bases.3• What is the molecular defects and pathophysiology of thalassemia 4• Describe the diagnostic test that detect genetic mutation of thalassemia 5• Overview of pre-marital screening test.Thalassemia and its genetic basis
The document provides information about thalassemia, including its types, causes, symptoms, identification tests, and treatment options. It begins with an introduction defining thalassemia as a hemoglobin disorder caused by defective synthesis of one or more globin chains. It then discusses the three main types - alpha thalassemia, beta thalassemia major/intermedia, and thalassemia minor. The document outlines the normal structure and function of hemoglobin, how mutations can disrupt this and cause thalassemia, and resulting organ dysfunctions. It details tests to identify thalassemia and standard treatment methods like blood transfusions, iron chelation therapy, and bone marrow transplants. Bioinformatics tools that
seminar on Thalassemia by Dr. habib Dr. mehadi Dr. asad
Dr. Habibur Rahman Bhuiyan and other doctors presented a seminar on thalassemia. They discussed a case of an 8-year-old boy with hereditary hemolytic anemia and symptoms of not growing well, pallor, and abdominal distension. The seminar covered the history, epidemiology, genetics, clinical presentations, complications, investigations, and management of different types of thalassemia including beta thalassemia major, beta thalassemia intermedia, HbE beta thalassemia, and alpha thalassemia. Investigations discussed included complete blood count, peripheral blood film, hemoglobin electrophoresis, and radiological imaging.
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Sickle cell anemia is a genetic blood disorder that affects red blood cells. It is most common among those of African descent. The disease causes red blood cells to become rigid and sickle-shaped, which can cause anemia, pain crises, and other serious complications. Symptoms vary from person to person but often include fatigue, shortness of breath, and pain. The disease is inherited when both parents carry the sickle cell trait, resulting in a 25% chance their child will have the disease.
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This document discusses thalassemia, an inherited blood disorder caused by missing or abnormal genes that affect hemoglobin production. It describes alpha and beta thalassemia specifically. Alpha thalassemia results from changes in genes for the alpha globin component and is most common in areas historically affected by malaria. Beta thalassemia is caused by a deficiency in beta globin production inherited in an autosomal recessive pattern. Symptoms range from mild anemia to severe anemia and organ enlargement. Treatment involves regular blood transfusions, iron chelation drugs, and sometimes splenectomy or bone marrow transplant.
Hemophila pp
Hemophilia is a genetic bleeding disorder caused by mutations on the F8 gene located on the X chromosome. People with hemophilia experience prolonged bleeding from minor injuries due to a lack of clotting factor VIII or IX in their blood. Treatment involves replacement therapy through frequent injections of clotting factor concentrates. While treatment allows people with hemophilia to live normal lives, risks include developing antibodies against the clotting factor and bleeding complications. Researchers are studying gene therapy as a potential cure by correcting the defective genes that cause hemophilia.
Genetic Disorders
Genetic disorders may be Mendelian and Chromosomal disorders.
example- Haemophilia, Sickle cell anemia, THalessemia, Colour Blindness, Phenylketonuria, Cystic fibrosis, Turner Syndromes etc
SICKLE CELL ANAEMIA IN PREGNANCY FOR MBBS UNDER GRADUATES OBG
Sickle cell anemia is caused by a point mutation that substitutes valine for glutamic acid in the beta globin chain of hemoglobin. This causes red blood cells to sickle under conditions of hypoxia, acidosis, cold, or dehydration. Sickling leads to hemolytic anemia and vaso-occlusive crises that can damage organs. Pregnancy further complicates sickle cell anemia by increasing risks of painful sickle cell crises, preeclampsia, and fetal growth restriction. Management involves preconception counseling, frequent monitoring during pregnancy for complications, and aggressive treatment of crises and infections to support a healthy pregnancy outcome.
Sickle cell anemia
Sickle Cell disease: is a genetic disorder that affects erythrocytes (RBC) causing them
to become sickle or crescent shaped.
The effects of this condition due to an abnormality of the hemoglobin molecules found
in erythrocytes.
Sickle cell anemia is a serious disease in which the body makes sickle-shaped red blood
cells. “Sickle-shaped” means that the red blood cells are shaped like a "C."
Normal red blood cells are disc-shaped and look like doughnuts without holes in the
center. They move easily through your blood vessels. Red blood cells contain the
protein hemoglobin. This iron-rich protein gives blood its red color and carries oxygen
from the lungs to the rest of the body.
Sickle cell Anemia is known as being a fatal hereditary form of anemia, it is recognized
by its abnormal red blood cells having a crescent shape due to the effect of hemoglobin
S found in the cells.
Thalassemia, blood,disorder,hemoglobin,red .cells
Thalassemia is a genetic blood disorder where the body produces unhealthy red blood cells and less hemoglobin. It is caused by mutations in the genes that make hemoglobin. There are two main types - alpha thalassemia and beta thalassemia. Symptoms include fatigue, weakness, and pale skin due to anemia. While there is no cure, treatment focuses on blood transfusions and chelation therapy to manage excess iron in the blood from the transfusions.
Sickle cell disease sandip
1. Sickle cell disease is an inherited blood disorder that affects hemoglobin and causes red blood cells to take on a sickle, or crescent, shape.
2. The prevalence of sickle cell disease varies by ethnicity, with the highest rates seen in African Americans at about 1 in 375 individuals.
3. Complications of sickle cell disease include anemia, infections, acute pain episodes, stroke, and damage to organs like the lungs, kidneys, spleen, and liver over time if not properly managed.
Anemia
Anemia is defined as a reduction in red blood cells or hemoglobin. It has many potential causes including blood loss, decreased bone marrow production, and genetic disorders. Symptoms include fatigue, palpitations, and shortness of breath. Diagnosis involves a complete blood count, peripheral smear, and identifying the underlying cause through history, examination, and additional testing. Treatment depends on the specific cause but may include iron supplementation, B12/folate, blood transfusions, or immunosuppressive drugs.
sickle cell anemia
Sickle cell anemia is an inherited form of anemia where red blood cells become rigid and shaped like sickles or crescents, due to a genetic mutation causing abnormal hemoglobin. Symptoms usually appear after 4 months and include abdominal pain, bone pain, breathing difficulties, fatigue, fever, and jaundice. Treatment focuses on managing symptoms, limiting crises, and taking folic acid supplements to support red blood cell production.
Klinefelter syndrome
Klinefelter syndrome is a genetic condition where males are born with an extra X chromosome, resulting in XXY. It can cause smaller testes and lower testosterone production, leading to reduced muscle and facial/body hair and enlarged breasts. It was first identified in 1942 in males with these symptoms. Testing hormone levels and chromosomes can diagnose it, and treatments aim to replace testosterone and address specific symptoms.
Oligospermia - Indira IVF
The point at which the male accomplice has low sperm count or under 15 million sperm for each ml in discharge due to Oligospermia, this impacts the male regenerative framework and can not prepare an egg. Accordingly female accomplice unfit to imagine pregnancy because of less sperm tally. Visit Indira IVF for appropriate direction to dispose of male infertility.
Hemophilia
This document provides information about hemophilia, including:
- Hemophilia is an inherited bleeding disorder caused by deficiencies in specific clotting factors like VIII or IX.
- There are three main types - A, B, and C - determined by which clotting factor is deficient.
- It is passed from parents to children via genes on the X chromosome.
- Symptoms include bruising and bleeding, especially into joints or muscles. Treatment aims to prevent bleeding complications through blood transfusions or replacement of the deficient clotting factor.
Fabry Disease Ppt.Cyrus & Jukie
Fabry disease is a rare genetic disorder caused by deficient activity of the enzyme alpha-galactosidase A. This enzyme breakdown lipids in the body. Its deficiency leads to a buildup of lipids in blood vessels, kidneys, and other organs. Symptoms include skin lesions, pain, kidney failure, and increased risk of heart disease. Treatment involves enzyme replacement therapy via intravenous infusion to help break down the buildup of lipids. However, this treatment does not cure the condition but only manages symptoms.
Clayton Perlman: What is Myelofibrosis?
Clayton Perlmanis no stranger to grief. He became a caretaker for his wife after she suffered from complications after a stem cell transplant for her myelofibrosis. After more than a year doing everything he could for his wife, she passed away from complications.
Thalassemia
Thalassemia is a genetic blood disorder characterized by defective or reduced hemoglobin. There are two main types: alpha thalassemia affects alpha globin chain production and beta thalassemia affects beta globin chain production. Symptoms range from mild anemia to severe anemia requiring regular blood transfusions depending on which genes are affected. Treatment involves lifelong blood transfusions combined with iron chelation therapy to prevent iron overload, and potentially splenectomy or bone marrow transplant.
Alpha thalassemia
presented by HAFIZ M WASEEM
university of education LAHORE Pakistan
i am from mailsi vehari and studied in lahore
Sickle Cell Anemia
Sickle cell Anemia is known as being a fatal hereditary form of anemia, it is recognized by its abnormal red blood cells having a crescent shape due to the effect of hemoglobin S found in the cells.
Post, Blog and Get Paid,
http://cashpaydaily.net
In the United States approximately 1 in every 375 African Americans are born with Sickle Cell Disease each year.
Sickle Cell Anemia is most common among people whose ancestors came from sub-Saharan Africa; Spanish-speaking regions in the Western Hemisphere (South America, the Caribbean, and Central America); Saudi Arabia; India; and Mediterranean countries such as Turkey, Greece, and Italy.
Sickle Cell Anemia occurs more often among people from parts of the world where Malaria is common.
Interesting Fact: People who have the sickle cell trait, (gene) are less likely to have severe forms of Malaria.
Home Base Business Opportunities
http://freedomofsuccess.com
A complete 8-Step 'Money Getting' Formula ($297 Value) In this High-Value Video Training Series, I'll learn the most effective ways to build a successful online business and the Core 'Must Have' principals to Effective Entrepreneurship in today’s market. These videos outline your BIGGEST money making principals all in one place Watch Video Here http://freedomofsuccess.com
anemia and thalassemia genetic bases ,the molecular defects and pathophysiol...
anemia and thalassemia genetic bases ,the molecular defects and pathophysiol...imam univarsity , college of medicine .
1• Define anemia and it's genetic bases.2• Describe thalassemia and it's genetic bases.3• What is the molecular defects and pathophysiology of thalassemia 4• Describe the diagnostic test that detect genetic mutation of thalassemia 5• Overview of pre-marital screening test.Thalassemia and its genetic basis
The document provides information about thalassemia, including its types, causes, symptoms, identification tests, and treatment options. It begins with an introduction defining thalassemia as a hemoglobin disorder caused by defective synthesis of one or more globin chains. It then discusses the three main types - alpha thalassemia, beta thalassemia major/intermedia, and thalassemia minor. The document outlines the normal structure and function of hemoglobin, how mutations can disrupt this and cause thalassemia, and resulting organ dysfunctions. It details tests to identify thalassemia and standard treatment methods like blood transfusions, iron chelation therapy, and bone marrow transplants. Bioinformatics tools that
seminar on Thalassemia by Dr. habib Dr. mehadi Dr. asad
Dr. Habibur Rahman Bhuiyan and other doctors presented a seminar on thalassemia. They discussed a case of an 8-year-old boy with hereditary hemolytic anemia and symptoms of not growing well, pallor, and abdominal distension. The seminar covered the history, epidemiology, genetics, clinical presentations, complications, investigations, and management of different types of thalassemia including beta thalassemia major, beta thalassemia intermedia, HbE beta thalassemia, and alpha thalassemia. Investigations discussed included complete blood count, peripheral blood film, hemoglobin electrophoresis, and radiological imaging.
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Sickle cell anemia is a genetic blood disorder where red blood cells become sickle-shaped and have difficulty passing through small blood vessels. This causes pain, organ damage, and risk of infection. It occurs most commonly in those with ancestry from sub-Saharan Africa, South America, the Caribbean, Mediterranean, and Middle East. Symptoms begin in early childhood and include anemia, pain crises, infections, and other complications. Treatment focuses on pain management, prevention of infections and complications, and new therapies are being researched.
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6..sickle cell anemia
Sickle cell anemia is a genetic blood disorder where red blood cells take on a sickle shape, clogging small blood vessels and leading to anemia. It is caused by the hemoglobin S gene and primarily affects those of African descent. Common symptoms include pain episodes, anemia, and increased infections. While there is no cure, treatments can help prevent complications and reduce pain through antibiotics, transfusions, and hydroxyurea. The only proven cure is bone marrow transplantation from a compatible donor.
Hemophilia
Hemophilia is a disease where the blood does not clot normally due to a defect in a gene controlling clotting. It is usually inherited from a parent and can develop in the womb by gene alterations. There are two main types based on low or missing clotting factor 8 or 9, with symptoms including uncontrollable bleeding and joint/pain issues. For serious cases, prevention is through regular clotting factor replacement therapy shots.
Hemophilia
Hemophilia is a disorder of the blood clotting system that prevents blood from clotting normally and stopping bleeding. It is caused by deficiencies in certain clotting factors, especially factors VIII and IX. Hemophilia is located on the X chromosome and is predominantly found in males, as they only have one X chromosome. Symptoms include abnormal bleeding and bruising, especially into joints and muscles. There is no cure for hemophilia, but regular injections of the missing clotting factor can control symptoms. Patients must take precautions to prevent injury but are encouraged to exercise and participate in normal activities.
Global Medical Cures™ | Blood disorders
Global Medical Cures™ | Blood disorders
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Global Medical Cures™ does not offer any medical advice, diagnosis, treatment or recommendations. Only your healthcare provider/physician can offer you information and recommendations for you to decide about your healthcare choices.
Student Work Sickle Cell
Sickle cell anemia is a blood disorder where red blood cells become stiff and form a crescent shape. It is inherited from parents, with risks of having the disease depending on if parents have the trait or full disease. Symptoms include pain, fatigue, infections, and organ damage. Treatments focus on pain management, antibiotics, and blood transfusions. It most commonly affects those with ancestry from regions where malaria is common.
Blood detectives consumer health discussion guide
Blood is vital to overall health, as it transports oxygen, fights infections, and connects to every organ. Understanding blood health and conditions is important, as problems can be detected with a blood test. The documentary profiles patients with common blood-related issues like anemia, bleeding disorders, blood clots, and cancers. It also shows researchers using tools like zebrafish to study these conditions and develop new treatments.
HAEMATOLOGY INTRODUCTION.pptx
Haematology is the study of blood, blood-forming organs, and blood diseases. Hematologists complete medical school and residency training before specializing in diagnosing and treating disorders like anemia, blood cancers, and bleeding disorders. Some key responsibilities of hematologists include understanding abnormalities in blood formation, diagnosing issues through lab tests, and managing care for patients with blood diseases. Common diseases treated include leukemia, myeloma, sickle cell anemia, and disorders affecting platelets or coagulation like hemophilia.
Sickle cell anemia
Sickle cell anemia is a genetic blood disorder where red blood cells become stiff and sticky and form clumps that can get stuck in blood vessels, blocking blood flow. This causes pain, infections, and organ damage. It occurs when someone inherits two sickle cell genes, one from each parent. Those with one sickle cell gene have sickle cell trait and do not have the disease. It most commonly affects those with ancestry from sub-Saharan Africa, South and Central America, the Caribbean, India, and Mediterranean countries. While there is no cure, treatments can help relieve symptoms and prevent complications.
Sickle Cell Anemia Essay
Sickel Cell Anemia Essay examples
Sickle Cell Anemia Essay
Sickle Cell Anemia Essay
Sickle Cell Disease Essay
Essay on Sickle Cell Anemia
Sickle Cell Anemia Essay
Sickle Cell Essay
Essay on Sickle Cell Anemia
Sickle Cell Anemia by Mohammed kareem
Sickle cell disease is a group of blood disorders typically inherited from one's parents where the oxygen-carrying protein hemoglobin is abnormal, causing red blood cells to take on a rigid, sickle shape. Problems typically begin around ages 5 to 6 and may include pain crises, anemia, infections, and organ damage. It is diagnosed through blood tests and affects those of African descent at much higher rates. Management focuses on preventing complications through medications, transfusions, and lifestyle changes.
Essay On Sickle Cell Anemia
The document provides information about sickle cell anemia. It discusses that sickle cell anemia is a genetic blood disorder where red blood cells become sickle shaped and have trouble flowing through small blood vessels. This causes tissue damage from lack of blood flow. Symptoms include anemia, pain episodes, organ damage, and stroke. It is inherited when both parents carry the sickle cell gene. While there is no cure, treatment focuses on managing pain and preventing complications.
Anemia (Investigatory project) class 11
Anaemia results from a lack of red blood cells or dysfunctional red blood cells in the body. This leads to reduced oxygen flow to the body's organs.
Symptoms may include fatigue, skin pallor, shortness of breath, lightheadness, dizziness or a fast heartbeat.
Treatment depends on the underlying diagnosis. Iron supplements may be used for iron deficiency. Vitamin B supplements maybe used for low vitamin levels. Blood transfusions may be used for blood loss. Medications to induce blood formation may be used if the body’s blood production is reduced.
TOOLBOX TALK | Stroke | Are you at risk?
Anyone can have a stroke, although there are some things that make you more at risk than others. It’s important to know what the risk factors are and do what you can to reduce your risk.
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Anemia that threatens women symptoms dangers - solution
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Waardenburg Syndrome
Waardenburg Syndrome is an inherited disorder characterized by hearing loss and changes in hair and skin pigmentation. There are four types, with types I and II being most common. It is caused by a dominant gene mutation and symptoms may include deafness, pale eye color, and patchy hair loss. While symptoms are present at birth, diagnosis is usually made in infancy through tests like audiometry and genetic testing. Treatment focuses on managing hearing loss and other symptoms, as there is no cure for the underlying condition.
Duchenne Muscular Dystrophy
Duchenne Muscular Dystrophy is a disease that causes rapidly worsening muscle weakness due to a lack of the protein dystrophin. It is inherited through an X-linked recessive gene, so it primarily affects boys. Symptoms begin in the legs and include fatigue, difficulty walking, and muscle weakness that gets worse over time and spreads to other muscles. There is no cure, and those affected often require use of a wheelchair by their early teens and don't survive past late teens or early adulthood.
Sickle Cell Anemia
Sickle cell anemia is a genetic blood disorder where red blood cells become stiff and sickle-shaped, blocking blood flow and damaging organs. It occurs when someone inherits two sickle cell genes, one from each parent. People with one sickle cell gene have sickle cell trait and do not have the disease but can pass the gene to their children. More than 70,000 Americans have sickle cell anemia and about 2 million have sickle cell trait. It is particularly common among African Americans, affecting about 1 in 12.
Williams Syndrome
Williams Syndrome is a rare genetic condition present at birth that affects physical features and development. It occurs in about 1 in 20,000 births due to a random genetic mutation. Common characteristics include heart defects, learning disabilities, an overly friendly demeanor, and narrow blood vessels. There is no cure for Williams Syndrome, but symptoms can be managed through careful medical care and avoiding excess calcium and vitamin D. The condition varies in severity and some cases, like that of Cody described, require multiple heart surgeries while allowing the person to live with milder ongoing effects of the syndrome.
Fibrodysplasia Ossifcans Progressiva
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare genetic disorder where muscle and connective tissue is gradually replaced by bone. It causes joints to become permanently frozen in place. While extra bone growth can be surgically removed, it will regrow. FOP is caused by a mutation that is inherited and passed down generations. Symptoms at birth may include great toes that are missing joints or have lumps. As the condition progresses, lumps and tumors develop on bones throughout the body. Currently there is no cure for FOP, and avoiding injury can help limit extra bone growth.
Marfan Syndrome
Marfan Syndrome is a connective tissue disorder that affects most organs and tissues, especially the lungs, eyes, and heart. It is caused by a defect in the gene that produces connective tissue and is inherited in an autosomal dominant pattern, meaning there is a 50% chance of passing it down to offspring. Symptoms include being unusually tall and thin with long limbs and fingers, as well as eye and heart problems. While there is no cure, treatment and surgery can help improve outcomes and lifespan. Famous Olympic swimmer Michael Phelps has Marfan Syndrome.
Huntington's Disease
Huntington's disease is a genetic disorder that causes certain nerve cells in the brain to break down over time. It is inherited in an autosomal dominant pattern, meaning only one parent needs to carry the gene for a child to be at risk. Common symptoms include behavioral changes, abnormal movements, dementia, and difficulty swallowing and speaking. While there is no cure, lifestyle interventions including diet, supplements, exercise and social support can help manage symptoms and potentially delay onset. The disease is caused by destruction of cells in the basal ganglia and approximately 1 in 33,333 people in the US are affected.
Achondroplasia
Achondroplasia is a genetic bone disorder that causes dwarfism. It results from a mutation affecting the formation of cartilage and bone and is characterized by short stature and limb abnormalities. Achondroplasia is inherited in an autosomal dominant pattern, but 80% of cases result from new mutations. It occurs in approximately 1 in 25,000 live births. While there is no cure for achondroplasia, limb lengthening surgery can help increase height in some patients.
Werners Syndrome
Werner syndrome is a rare genetic disorder characterized by premature aging symptoms beginning in early adulthood such as graying hair, a thin body build, and bird-like facial features. It is caused by mutations in the WRN gene and inherited in an autosomal recessive pattern. People with Werner syndrome typically die of heart disease or cancer in their late 40s or early 50s as their bodies age at an accelerated rate. There is no cure for Werner syndrome, but managing health conditions like diabetes and monitoring cholesterol levels is recommended.
Williams Syndrome
Williams Syndrome is a rare genetic disorder caused by a deletion of genes on chromosome 7, resulting in physical, cognitive, and behavioral effects including distinctive facial features, learning difficulties, and anxiety. It is not typically inherited but occurs randomly during reproduction. While there is no cure, treatment may include physical, speech, and occupational therapy as well as managing blood pressure and calcium levels.
Achondroplasia
Achondroplasia is a genetic condition that results in abnormally short limbs and an enlarged head. It is caused by mutations in the FGFR3 gene. Symptoms include bowed legs, prominent forehead, and abnormal finger spacing. While there is no cure, treatment focuses on supportive care and monitoring for potential spinal issues. The condition can be diagnosed before or after birth based on physical features and imaging tests.
Werners Syndrome
Werner syndrome is a rare genetic disorder that causes accelerated aging beginning in early adulthood. It is caused by mutations in the WRN gene and is inherited in an autosomal recessive pattern. Physical symptoms include short stature, gray hair, cataracts, skin aging, and increased risk of cancers and heart disease. There is no treatment to stop or reverse the effects of Werner syndrome, but symptoms can be managed.
Fibrodysplasia Ossifican Progressiva
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare genetic disorder where muscle tissue and connective tissue are gradually replaced by bone. It is caused by a mutation in the body's repair mechanism, causing extra bone to form following injuries. There is no treatment for FOP, and surgery can make it worse by triggering more bone growth. Most cases are caused by spontaneous genetic mutations, and those affected have very limited mobility as the condition progresses and more joints become frozen in place by extra bone formation.
Tay Sachs Disease
Tay-Sachs disease is a rare genetic disorder where harmful amounts of fat build up in nerve cells, causing seizures, loss of skills, and eventual death by age 5 in most cases. It is inherited when both parents carry a mutated gene and have a 25% chance of passing it to their child. Symptoms appear before 6 months of age and include losing abilities like smiling, crawling, and eye contact. Currently there is no cure, though supportive treatments can help manage symptoms. Testing for carriers is done with a blood test.
Sickle Cell
Sickle cell disease is an inherited blood disorder where red blood cells become misshapen and crescent-shaped. It causes episodes of pain and other symptoms like fatigue and jaundice. While there is no cure, treatment with medication can help manage symptoms though the disease remains. It is most common among those with ancestry from sub-Saharan Africa, South and Central America, Caribbean countries, and Mediterranean countries.
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Hemophilia
- 1. Hemophilia By: Cody Mengel Cory Waddingham
- 2. What It Is Hemophilia is a disease where your blood is too thin and you blood can’t clot
- 3. How it’s inherited Hemophilia is a sex-linked disease. It is inherited through family. Mostly males get this disease. Its very rare for females to get it.
- 4. Symptoms The main symptom is bleeding. The bleeding usually won’t stop when you get cut.
- 5. How this disease is diagnosed Hemophilia is tested after you notice that you have a hard time clotting. You’d go to the doctor’s and they will tell you if you have it It is also likely when there is a history of this disease in your family.
- 6. Occurrence 18,000 people in the United States have this disorder. Each year about 400 babies are born in the United States with this disorder.
- 7. Treatment It is treatable by replacing the missing clotting factors by injecting special fluids into the veins This will help your blood clot easier
- 8. Other Interesting Info. You can bleed to death from a small cut. You can bleed to death internally too.
- 9. Personal Story Kristy Dobson is an 18 year figure skater from Canada with Hemophilia She says when her ankle sprained it took months to finally heal She also says when she bends her arm she breaks many blood vessels
- 10. Work Cited Google health (hemophilia) http://www.sciencecases.org/hemo/hemo.asp http://www.hemophilia.ca/en/our-stories/kristy---how-a-bleeding-disorder-has-affected-my-life/