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  • Tahukah Anda Apa Itu Thalasemia ?

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    Virnadia Ekasari Andriani
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    Thalassemia is a hereditary blood disorder characterized by a deficiency in the production of the globin chains that make up hemoglobin. There are two types of thalassemia - alpha and beta thalassemia. Beta thalassemia involves a reduction or absence of beta globin chain production, leading to increased compensatory production of other chains and abnormal hemoglobin. Symptoms include fatigue, paleness, weakness, lack of appetite, shortness of breath, enlarged spleen and thinning of bone cartilage. Treatment options include blood transfusions, chelating agents, spleen removal, and bone marrow transplants for severe cases of beta thalassemia.

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    Thalassemia is a hereditary blood disorder characterized by a deficiency in the production of the globin chains that make up hemoglobin. There are two types of thalassemia - alpha and beta thalassemia. Beta thalassemia involves a reduction or absence of beta globin chain production, leading to increased compensatory production of other chains and abnormal hemoglobin. Symptoms include fatigue, paleness, weakness, lack of appetite, shortness of breath, enlarged spleen and thinning of bone cartilage. Treatment options include blood transfusions, chelating agents, spleen removal, and bone marrow transplants for severe cases of beta thalassemia.

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    5 views2 pages

    Tahukah Anda Apa Itu Thalasemia ?

    Uploaded by

    Virnadia Ekasari Andriani
    Thalassemia is a hereditary blood disorder characterized by a deficiency in the production of the globin chains that make up hemoglobin. There are two types of thalassemia - alpha and beta thalassemia. Beta thalassemia involves a reduction or absence of beta globin chain production, leading to increased compensatory production of other chains and abnormal hemoglobin. Symptoms include fatigue, paleness, weakness, lack of appetite, shortness of breath, enlarged spleen and thinning of bone cartilage. Treatment options include blood transfusions, chelating agents, spleen removal, and bone marrow transplants for severe cases of beta thalassemia.

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    of 2

    Tahukah anda apa terdiri dari dua rantai alpa

    dan beta polipeptide.


    itu thalasemia ?
    Dalam beta thalasemia ada
    Thalasemia adalah penurunan sebagian atau
    suatu gangguan darah keseluruhan dalam proses
    yang diturunkan yang sintesis molekul
    ditandai oleh defisiensi hemoglobin rantai beta
    produksi rantai globin dan mengakibatkan
    pada hemoglobin. peningkatan compensatori
    THALASEMIA
    Thalasemia adalah dan menyebabkan
    kerusakan sel darah merah ketidaksempurnaan
    Disusun oleh : didalam pembuluh darah perubahan hemoglobin.
    Polipeptid yang tidak
    Firlaili Laila .R seimbang dapat
    Penyebab
    Nur Purnama .S menyebabkan anemia
    1. Factor keturunan yang parah
    Virnadia Eka .S

    Proses Terjadinya
    Hemoglobin paska
    kelahiran yang normal
    AKADEMI KEPERAWATAN
    WILLIAM BOOTH
    SURABAYA
    Tanda dan gejala
     Letargi
     Pucat
     Kelemahan
     Tidak napsu makan
     Sesak nafas
     Tebalnya tulang kepala
     Pembesaran limpa
     Menipisnya tulang
    kartilago

    Penanganan
    1. Transfusi sel darah
    merah
    2. Pemberian chelating
    agents (Desferal
    3. Tindakan splenektomi
    4. Transplantasi sumsum
    tulang biasa dilakukan
    pada thalasemia beta
    mayor.

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