Thalassemias slide 1 by the end of the lecture, the. Thalassemia womens and infants health at mount sinai. Thalassemia is due to a deficit or absent production of. This is called the cis form of alpha thalassemia trait. Dec 16, 2019 patients with severe beta thalassemia are dependent on red cell transfusions either regularly thalassemia major or intermittently thalassemia intermedia. Alpha thalassemia nord national organization for rare. Thalassemias are a group of inherited microcytic, hemolytic anemias characterized by defective hemoglobin synthesis. In this type, the lack of beta protein causes no problems in the normal functioning of the hemoglobin. Confirmation of alphathalassemia trait can be hard, since hb electrophoresis is normal, but commercially available polymerase chain reaction pcr screening for. The different types of hemoglobin present at different ages. Thalassemia patofisiologi, diagnosis, penatalaksanaan. Thalassemias blood disorders merck manuals consumer version. Thalassemia intermedia is a less serious kind of betathalassemia and do not require the patient to go through blood transfusions.
Pathophysiology and clinical manifestations of the bthalassemias arthur w. A person with this condition simply carries the genetic trait for thalassemia with no health problems other than a possible mild anemia cooleys anemia foundation, 2010. Betathalassemia genetic and rare diseases information. In beta thalassemia major sometimes called cooley anemia, people have severe symptoms of anemia, such as fatigue, weakness, and shortness of breath, and they may also have jaundice, causing yellowing of the skin and whites of the eyes, skin ulcers, and gallstones. Individuals with alpha thalassemia, particular the intermediate or severe forms, will benefit from referral to a thalassemia treatment center. In all cases a failsafe system must be in place to make sure all eligible women have been offered screening, and those that accept are tested. Satu dari orang tua menderita thalasemia traitbawaan maka kemungkinan 50% sehat dan 50% thalasemia trait. High prevalence trusts are considered high prevalence if 2% or more of the booking bloods are. Thalassemia trait is commonly detected when routine peripheral blood smear and complete blood count show microcytic anemia and elevated red cell count. If desired, the diagnosis of beta thalassemia trait can be confirmed with quantitative hemoglobin studies. Slide hemoglobin h disease y second most severe form alpha thalassemia. Alpha thalassemia mental retardation syndrome can be caused by a deletion of a significant amount of chromosome 16, affecting the alpha globin genes. Please use one of the following formats to cite this article in your essay, paper or report.
Total score ranges from 0 to 3,600 being 0 the worst and 3,600 the best. Patofisiologi yang mendasari antara jenis thalassemia hampir sama, ditandai dengan penurunan produksi hemoglobin dan sel darah merah rbc, adanya kelebihan rantai globin yang tidak efektif, akan menyebabkan bentuk homotetramers yang tidak stabil sehingga memicu terjadinya. Beta thalassemia is an inherited blood disorder in which the body doesnt make hemoglobin normally. Over the years, we have seen significant advances in medical technology, including assessment, monitoring and therapy for thalassemia. Regardless of their transfusion needs, such patients should be followed at a thalassemia comprehensive care center under the care of a hematologist, so that they can be monitored for short and longterm complications of chronic. Pathophysiology and clinical manifestations of the. Slide 1 thalassemias slide 2 lecture outline by the end of the lecture, the student should know.
Despite discoveries concerning the molecular abnormalities that led to the thalassemic syndromes, it still is not known how accumulation of excess unmatched alphaglobin in beta thalassemia and betaglobin in alpha thalassemia leads to red blood cell hemolysis in the peripheral blood, and in the beta thalassemias particularly, premature. Proses pembuahan, anak hanya mendapat sebelah gen globin beta dari ibunya dan sebelah lagi dari ayahnya. Pada thalassemia alfa, gen untuk terbentuknya rantaii globin alfa adalah yang terpengaruhi, dan kebalikannya untuk thalassemia beta. Thalassemia in arab populations alpha and beta thalassemia are endemic in almost all arab countries probably due to the historical presence of malaria in the region and the high level of consanguinity. These carriers may be still easily identified because they have the typical increase of hba 2 levels. Beta thalassemia is more common among people of mediterranean, middle eastern, southeast asian, or indian ancestry. Most children with thalassemia major appear healthy at birth but, during the first year or two of life, they become. In betathalassemia major sometimes called cooley anemia, people have severe symptoms of anemia, such as fatigue, weakness, and shortness of breath, and they may also have jaundice, causing yellowing of the skin and whites of the eyes, skin ulcers, and gallstones. The trans and cis types of alpha thalassemia trait are found most often in people whose ancestors come from southeast asia, southern china, the mediterranean, and the middle east. Patofisiologi thalassemia mencakup mutasi atau delesi pada gen untuk rantai globin alfa ataupun beta. Alpha thalassemia is particularly common among people of african, mediterranean, or southeast asian ancestry.
The increase in number of patients with thalassemia living in california highlights the importance of provider knowledge about thalassemia in order to effectively serve these patients in their communities. The name is derived from the greek word thalassa meaning the sea because the condition was first described in populations living near the mediterranean sea. Finally, healthrelated quality of life is discussed in these patients with a direct comparison to the more severe. Healthy living centers for disease control and prevention also in spanish. Although most are small nucleotide substitutions within the cluster, deletions may also cause b thalassemia. Thalassemia is an inherited disease of faulty synthesis of hemoglobin. Thalassemia definition thalassemia describes a group of inherited disorders characterized by reduced or absent amounts of hemoglobin, the oxygencarrying protein inside the red blood cells.
Nutrition and diet northern california comprehensive thalassemia center thalassemia centers for disease control and prevention thalassemia. Alpha thalassemia is a general term for a group of inherited blood disorders characterized by reduced or absent production of alphaglobin subunits, resulting in low levels of hemoglobin that is otherwise fully functional. Pada negara tropikal membangun, elektroporesis bisa juga mendeteksi hb c, hb s dan hb j wiwanitkit, 2007. Pengobatan penyakit thalassemia sampai saat inibelum sampai pada tingkat penyembuhantransplantasi sumsum tulang. This is usually not inherited, but rather occurs sporadically in. There are two basic groups of thalassemia disorders. For instance, if a person receives a beta thalassemia trait from his father and another from his mother, he will have beta thalassemia major. Rucknagel department of human genetics, university of michigan medical school, ann arbor, michigan previous contributors to this symposium have defined thalassemia in. Diagnosis thalassemia thalassemia alpha tidak semua jenis thalassemia alpha dapat didiagnosis dengan pemeriksaan hematologi indeks sel darah merah, morfologi sel darah merah dan analisis hb yang selalu dapat didiagnosis dengan pemeriksaan hematologi. Symptoms soulmates are people with similar symptoms to you. Thalassemia secara umum dapat dibagi menjadi thalassemia alfa dan beta. Carrier frequencies of beta thalassemia vary from 1% to 5% while prevalence data for alpha thalassemia are scant.
Beta thalassemia minor, which is a mild, nontransfusion dependent anemia is caused by a defect in one copy of the beta gene. Pada saat molekul hemoglobin mengangkut dan melepas o 2, masingmasing rantai. Thalassemia australia pdf ppt case reports symptoms. Thalassemia termasuk hemoglobinopati djelantik, 1996. It effects as many as 1 in 30 pregnancies in china, india, and pakistan, 1 in 100 pregnancies in thailand, and 1 in pregnancies in northern europe and the united states. Hemoglobin a hba mencakup 9598% dari seluruh jumlah hemoglobin pada tubuh dan terdiri dari tetramer yang terbuat dari 2 subunit globin alfa dan 2 subunit globin beta. This is a power point presentation titled thalassemia. Family history and ancestry are factors which increase the risk of beta thalassemia. Beta thalassemia trait is found in individuals where there is only one hbb gene mutation in each cell possess mild anaemia.
Jude childrens research hospital, memphis, tennessee 38105 2department of pediatric oncology, danafarber cancer institute, and the division of hematology and oncology, childrens hospital, boston, massachusetts 02215. Aug 23, 2018 thalassemia is a blood disorder that is caused by dna mutations in cells that are responsible for producing haemoglobin. Patients with severe beta thalassemia are dependent on red cell transfusions either regularly thalassemia major or intermittently thalassemia intermedia. Betathalassemia is more common among people of mediterranean, middle eastern, southeast asian, or indian ancestry. If one parent has the cis form of alpha thalassemia trait, and the other parent is a silent carrier. Betathalassemia major and betathalassemia intermedia are usually inherited in an autosomal recessive manner, which means both copies of the hbb gene in each cell have mutations. Alpha thalassemia trait normally does not cause any health problems. Guidelines for the clinical care of patients with thalassemia in canada. The clinical manifestations include hemolytic anemia and impaired iron handling, the severity of which depends on the degree of impairment in beta globin production. Dec 12, 2011 thalassemia thalassemia is an inherited blood disorder in which the body produces an abnormal form of hemoglobin which results in excessive destruction of red blood cells and further leads to anemia. Thalassemia minor also called thalassemia trait may cause no symptoms, but mild anemia and other changes in the blood do occur. Thalassemia thalassemia is an inherited blood related disorder due to absent or reduced production of hemoglobin, a protein present in red blood cells responsible for carrying oxygen through the body. The abnormal hemoglobin can lead to anemia not enough rbcs in the body and other medical problems.
Hemoglobin pada dewasa terdiri dari bentuk a, a2 dan f fetal. Thalassemia is a blood disorder that is caused by dna mutations in cells that are responsible for producing haemoglobin. Pathophysiology and clinical manifestations of the bthalassemias. Such individuals carry the diagnosis of thalassemia major. Thalassemia major is the most severe form of beta thalassemia. Alpha thalassemia thal uh see mee uh trait is a condition that affects the amount of hemoglobin in the red blood cells. The clinical phenotype results from both the diminished amount of the particular globin chain as well as from the resultant chain imbalance that occurs because of normal production of the other globin chain. Hbbart hydrops fetalis yang disebabkan oleh delesi ke4 gen globin alpha beberapa jenis penyakit hbh. This kind of thalassemia is so serious that it needs frequent blood transfusions. This leads to a reduction in the number and ability of the red blood cells to carry oxygen throughout the body and can cause sufferers to feel symptoms such as fatigue. If your parents have missing or altered hemoglobinmaking genes, you may have thalassemia. When two carriers have children, each child has a 25% 1 in 4 chance to be. Campbell, md louisiana state university health sciences center, new orleans, louisiana t he thalassemias named from the.
Feb 26, 2019 please use one of the following formats to cite this article in your essay, paper or report. Alpha thalassemia trait all red blood cells contain hemoglobin hee muh glow bin, which carries oxygen from your lungs to all parts of your body. Beta thalassemia is an inherited hemoglobinopathy in which the production of one or both beta globin chains is impaired. Hemoglobin is the part of red blood cells rbcs that carries oxygen throughout the body. Thalassemias national heart, lung, and blood institute. Scribd is the worlds largest social reading and publishing site. Nhs sickle cell and thalassaemia screening programme 7 trusts merge the high prevalence algorithm should be used. This leads to a reduction in the number and ability of the red blood cells.
Pathophysiology and clinical manifestations of the b. Thalassemia thalassemia is an inherited blood disorder in which the body produces an abnormal form of hemoglobin which results in excessive destruction of red blood cells and further leads to anemia. Aug 09, 2019 the increase in number of patients with thalassemia living in california highlights the importance of provider knowledge about thalassemia in order to effectively serve these patients in their communities. Thalassemia is seemingly the most common genetic abnormality in the world. Depending on family history, if a persons parents or grandparents had beta thalassemia major or intermedia, there is a 75% 3 out of 4 probability see inheritance chart at top of page of. Find your symptoms soulmates from now on you can add your symptoms in diseasemaps and find your symptoms soulmates. Each red blood cell may contain between 240 and 300 million molecules of hemoglobin. This is the most severe form of beta thalassemia in which there is complete lack of beta protein in the hemoglobin, which causes a lifethreatening anemia that requires regular blood.
Complications in thalassaemia patients receiving blood tranfusion hira tahir1,syeda amna shahid1,khawaja tahir mahmood2. Real stories of people living with thalassemia centers for disease control and prevention also in spanish. Betathalassemia trait is found in individuals where there is only one hbb gene mutation in each cell possess mild anaemia. Athalassemia definition of athalassemia by medical. People with alpha thalassemia trait do not develop hemoglobin h disease or hydrops fetalis later in life. Thalassemia medical powerpoint presentation download. Hemoglobin h diseaselike symptoms can also be a part of a unique condition called alpha thalassemia mental retardation syndrome. Alpha thalassemia pregnancies are rising in north america and require prenatal counseling, overall community education, and welldeveloped intrauterine management plans. Basic features of thalassemia syndromes transfusion protocols in thalassemia chelation therapy in thalassemia supportive care in thalassemic patients followup guidelines hemtopoitic stem cell transplantation future aspects. Number of newly diagnosed thalassaemia major cases per annum. People with hemoglobin h disease can have an enlarged spleen, low red blood. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Thalassemias slide 1 by the end of the lecture, the student. Thalassemias occur most often among people of italian, greek.
Jude childrens research hospital, memphis, tennessee 38105 2department of pediatric oncology, danafarber cancer institute, and the division of hematology and. Fiftysix patients were followed up with diagnosis of thalassemia major and 11 with thalassemia intermedia. Eritrosit dalam darah arteri sistemik mengangkut o 2 dari paru ke jaringan dan kembali dalam darah vena dengan membawa co 2 ke paru. Alphathalassemia is particularly common among people of african, mediterranean, or southeast asian ancestry. If both parents have the trans form of alpha thalassemia trait. Laboratory diagnosis of hemoglobinopathies and thalassemia. Thalassemia nearly 200 different mutations have been described in patients with bthalassemia and related disorders. Athalassemia definition of athalassemia by medical dictionary. Nhs sickle cell and thalassaemia screening programme. Thalassemias are inheritedthat is, the genes for the disorders are passed from parents to their children. Alpha thalassemia results from large deletions in the alpha genes.
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