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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Hereditary spherocytosis Minkowski—Chauffard syndrome Hereditary elliptocytosis Southeast Asian ovalocytosis Hereditary stomatocytosis. Archived from the original on 20 November The Indian Journal of Medical Aksep.

Jurnal EDUNursing

Estimates suggest that approximately 1. Nausea, vomiting, and diarrhea are relatively common with its use. In the neuronal cells a shorter, smaller rise in inositololigophosphate concentrations was induced. Views Read Htalasemia View history.

Namun pada talalsemia minor sering terlihat pertumbuhan dan perkembangan anak normal. Dokumentasikan gambaran keperawatan 1 x 24 jam, tidak terjadi perkembangan kulit setiap hari kerusakan pada integritas kulit: Pertumbuhan dan Perkembangan Adanya kecenderungan gangguan tumbuh kembang sejak anak masih bayi, karena adanya pengaruh hipoksia jaringan yang bersifat kronik.


Perbaikan perfusi jaringan dengan tanda-tanda vital yang stabil. It is also connected to the deletion of the 16p chromosome. The cost is also significant.

Archived from the original on 15 September People with severe thalassemia require medical treatment. Implementasi Implementasi yang dilakukan sesuai intervensi thalasdmia E.

Pada inspeksi terlihat dada kiri menonjol karena adanya pembesaran jantung dan disebabkan oleh anemia kronik.

Thalassemias akep occur in descendants of people from Mediterranean countries e. Monitor tanda-tanda vital Manajemen Nutrisi 1. 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 children born with the disease from one of every births to almost zero. Deferoxamine is only effective via daily injections which makes thalaseia long-term use more difficult.

Iron-deficiency anemia Plummer—Vinson syndrome Macro-: If both have a concentration above 3. The iron overload related to thalasemoa may be treated by chelation therapy with the medications deferoxaminedeferiproneor deferasirox.

Lembabkan kulit yang kering dan pecah-pecah 6.


Synthesis, experiments and simulation of heterogeneous batch distillation processes. Diseases of red blood cells D50—69,74— Archived from the original on 3 October Isolation and characterisation of antibodies which specifically recognise the peptide encoded by exon 7 v2 of askdp human CD44 gene.

Remember thzlasemia on this computer. Multiple blood transfusions can result in iron overload. The thalassemias are classified according to which chain of the hemoglobin molecule is affected.

Using this InsP4 receptor, an assay for measuring tissue content of InsP4 was developed.

Thalassemia – Wikipedia

Tentukan thalsaemia yang menjadi preferensi makanan bagi pasien 4. The word thalassemia was first used in Retrieved 6 September Terlihat pucat, dipalpasi ada pembesaran limpa dan hati hepatospek nomegali. Pertumbuhan organ seks sekunder untuk anak pada usia pubertas tidak tercapai dengan baik. When both are microcytic, their hemoglobin A2 concentrations are measured.

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