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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Inin Spain, a baby was selectively implanted to be a cure for his brother’s thalassemia.

Two gene loci and so four alleles exist. Retrieved from ” https: American Society of Hematology. Kecerdasan anak juga mengalami penurunan. Williams Hematology 9e ed.

Hindarkan kulit kelembaban dari berlebih yang berasal dari keringat 4.

Thalassemia

In the same tissue samples the amount of Ins 1,4,5 P3 was determined in parallel with a similar assay using a binding protein preparation from beef liver.

For the autosomal recessive forms of the disease, both parents must be carriers for a child to be affected. In Europe, the highest concentrations of the disease are found in Greececoastal regions in Turkey particularly the Aegean Region such as IzmirBalikesirAydinMuglaand Mediterranean Region such as AntalyaAdanaMersinin parts of Italyparticularly southern Italy and the lower Po valley.

The beta form of thalassemia is particularly prevalent among Mediterranean peoples, and this geographical association is responsible for its original name. Observasi adanya petunjuk non verbal mengenai ketidak menggunakan – tindakan pencegahan Secara mereka konsisten terutama yang tidak pada dapat tindakan berkomunikasi secara efektif 3.

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Blood tests, genetic tests [3]. Hal ini terjadi terutama unutk talasemia mayor. Sehinga berat badan anak akan sangat rendah dan tidak sesuai dengan usianya. Pasang bantalan pada siku dan tumit jika dibutuhkan 8. Tentukan jumlah kalori dan jenis nutrisi yang dibutuhkan untuk memenuhi persyaratan thqlasemia 2.

The most common of these are:.

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This page was last edited on 21 Novemberat Indian Journal of Endocrinology and Metabolism. Ins 1,4,5 P3 and other inositol phosphates were less effective. The cost is also significant. Thalassemia can coexist with other hemoglobinopathies. The New England Journal of Medicine.

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Riwayat Kesehatan Keluarga Talasemia merupakan penyakit keturunan, maka perlu dikaji apakan ada orang tua yang menderita talasemia. Iron-deficiency anemia Plummer—Vinson syndrome Macro-: Enter the email address you signed up with thalaesmia we’ll email you a reset link. Pastikan intake nutrisi yang cukup terutama protein, vitamin B dan C, besi, dan kalori, dengan menggunakan suplemen yang tepat 3.

Ketidak efektifan asskep jaringan perifer Setelah NOC dilakukan tindakan Manajemen keperawatan 2 x 24 jam, terjadi 1. Monitor tanda-tanda vital Manajemen Nutrisi 1. The major Mediterranean islands except the Balearics such as SicilySardiniaMaltaCorsicaCyprusand Crete are heavily affected in particular.

Click here to sign up. Views Read Edit View history. Namun pada talalsemia minor sering terlihat pertumbuhan dan perkembangan anak normal. Pola Makan Karena adanya anoreksia sehingga anak sering mengalami susah makan. Journal of Bone and Mineral Research.

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Archived from the original on 4 December As ofthalassemia occurs in about million people, with abouthaving severe disease. Am J Dis Child ; Thalassemias also occur in descendants of people from Mediterranean countries e. D ICD – Current Opinion in Obstetrics and Gynecology. Thalawemia from the original on The HSCs then have a beta-globin gene added using a lentiviral vector.

Ketidak efektifan perfusi jaringan perifer 2. After destroying the affected person’s bone marrow with a dose of hhalasemia a myeloablative conditioning regimenthe altered HSCs are infused back into the affected person thalsemia they become engrafted in the bone marrow where they proliferate. Kulit dan mulai dari hari pertama dirawat Setelah NOC dilakukan Membran Mukosa – Perfusi jaringan tidak terganggu – Integritas kulit tidak – terganggu Tidak ada lesi pada kulit Tidak ada pigmentasi abnormal 2.

Megaloblastic anemia Pernicious anemia. A screening policy exists in Cyprus to reduce the rate of thalassemia, which, since the program’s implementation in the s which also includes prenatal screening and abortionhas reduced the number of xskep born with the disease from one of every births to almost zero. It however is not effective in everyone and is probably not suitable in those with significant cardiac issues related to iron overload.