Askep Thalasemia Ela – Download as Word Doc .doc /.docx), PDF File .pdf), Text File .txt) or read online. The PDF file you selected should load here if your Web browser has a PDF reader plug-in installed (for example, a recent version of Adobe Acrobat Reader). Thalassemias are inherited blood disorders characterized by abnormal hemoglobin production. Symptoms depend on the type and can vary from none to severe.

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Archived from askpe original on 26 August Having a single genetic variant for thalassemia may protect against malaria and thus can be an advantage.

Iron-deficiency anemia Plummer—Vinson syndrome Macro-: In the glioma cells the concentrations of both inositol 1,4,5-trisphosphate and inositol 1,3,4,5-tetrakisphosphate were raised about 2.

Treatment depends on the type and severity. Archived from the original on 20 November Pertumbuhan dan Perkembangan Adanya kecenderungan gangguan tumbuh kembang sejak anak masih awkep, karena adanya pengaruh hipoksia jaringan yang bersifat kronik.

azkep Large scale awareness campaigns are being organized in India [30] both by government and non-government organizations in favor of voluntary premarital screening to detect carriers of thalassemia and marriage between both carriers are strongly discouraged. They should avoid routine use of iron supplements ; iron deficiency can develop, though, during pregnancy or from chronic bleeding.


Thalassemia – Wikipedia

Pada inspeksi terlihat dada kiri menonjol karena adanya pembesaran jantung dan disebabkan oleh anemia kronik. The transplantation was considered successful.

Archived from the original on 4 Askkep Pasang bantalan pada siku dan tumit jika dibutuhkan 8. Am J Dis Child ; Estimates suggest that approximately 1.

By using this site, you agree to the Terms of Use and Privacy Policy. Genetic disorders inherited [2]. In Europe, the highest concentrations of the disease are found in Greececoastal regions in Turkey particularly the Aegean Region such as IzmirBalikesirAydinAzkepand Mediterranean Region such as AntalyaAdanaMersinin parts of Italyparticularly southern Italy and the lower Po valley.

As ofthalassemia occurs in about million people, with about askrp, having severe disease. D ICD – It however is not effective in everyone and is probably not suitable in those with significant cardiac issues related to iron overload.

Riwayat Kesehatan Keluarga Talasemia merupakan penyakit keturunan, maka perlu dikaji apakan ada orang tua yang menderita talasemia. Pastikan perawatan analgesic tanpa bagi pasien dilakukan dengan analgesic Secara konsisten melaporkan pemantauan yang ketat 4. The major Mediterranean islands except the Balearics such as Sicily aske, SardiniaMaltaCorsicaCyprusand Crete are heavily affected in particular. There is no evidence from randomized controlled trial to support zinc supplementation in thalassemia.


Jurnal EDUNursing

Misal tidak tumbuh rambut ketiak, pubis ataupun kumis bahkan mungkin anak tidak dapat mencapai tapa odolense karena adanya anemia kronik. Williams Hematology 9e ed. The Challenge of Thalassemia for the Developing Countries”.

In the neuronal cells a shorter, smaller rise in inositololigophosphate concentrations was induced. Monitor tanda-tanda vital Manajemen Nutrisi 1.


Pastikan intake nutrisi yang cukup terutama protein, vitamin B dan C, besi, dan kalori, dengan menggunakan suplemen yang tepat 3. Synthesis, experiments and simulation of heterogeneous batch distillation processes. Archived from the original on Autosomal recessive disorders Hereditary hemolytic anemias Disorders of globin and globulin proteins.

Riwayat Ibu Saat Hamil Selama kehamilan perlu dikaji adanya factor risiko talasemia. Deferoxamine is only effective via daily injections asksp makes its long-term use more difficult. Gene therapy is being thalasemiw for thalassemia. Indian Journal of Endocrinology and Metabolism. Feeling tiredpale skinenlarged spleenyellowish skindark urine [1].