ASKEP THALASEMIA PDF

ASKEP THALASEMIA PDF

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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Treatment depends on the type and severity. The severity of the disease depends on the nature of the mutation and on the presence of mutations in one or both alleles. Click here to sign up. Estimates suggest that approximately 1. Genetic disorders inherited [2].

Thalassemia

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Diseases of red blood cells D50—69,74— Tentukan jumlah kalori thalasmia jenis nutrisi yang dibutuhkan untuk memenuhi persyaratan gizi 2. Annals of Tropical Medicine and Parasitology.

Isolation and characterisation of antibodies which specifically recognise the peptide encoded by exon 7 v2 of the human CD44 gene. Thalassemias are inherited blood disorders characterized by abnormal hemoglobin production. Riwayat Kesehatan Anak Anak cenderung mudah terkena infeksi saluran nafas bagian atas atau infeksi lainnya.

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Pola Makan Karena adanya anoreksia sehingga anak sering mengalami susah makan. The iron overload related to thalassemia may be treated by chelation therapy with the medications deferoxaminedeferiproneor deferasirox. Hal ini terjadi karena adanya penumpukan zat besi dalam jaringan kulit hemosiderosis. Ads help cover our server costs.

The Indian Journal of Medical Research.

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.

Berikan cairan yang sesuai 5. In some developing countries, there are virtually no facilities for diagnosis or management of thalassemia. 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. Lembabkan kulit yang kering dan pecah-pecah 6.

Intruksikan pasien mengenai kebutuhan nutrisi 5. In the glioma cells the concentrations of both inositol 1,4,5-trisphosphate and inositol 1,3,4,5-tetrakisphosphate were raised about 2. This potentially results in a progressive increase in hemoglobin A2 synthesis in all subsequent developing red blood cells, with resultant resolution of the anemia. Mata dan konjungtiva pucat dan kekuningan d. Hereditary spherocytosis Minkowski—Chauffard syndrome Hereditary elliptocytosis Southeast Asian ovalocytosis Hereditary stomatocytosis.

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Berikan informasi mengenai menggunakan pengurangan – nyamanan nyeri nyeri yang terkontrol nyeri, seperti penyebab nyeri, talasemia lama nyeri akan dirasakan, dan antisipasi dari ketidak nyamanan akibat prosedur 5. Just as with beta thalassemia, mutations that affect the ability of this gene to produce delta chains can occur. The transplantation was considered successful. Kepala dan bentuk muka Anak yang belum mendapatkan pengobatan mempunyai bentuk khas, yaitu kepala membesar dan muka mongoloid hidung pesek tanpa pangkal hidungjarak mata lebar, tulang dahi terlihat lebar.

Askep Teori Thalasemia Nic Noc – PDF Free Download

Archived from the original on 25 February Views Read Edit View history. Greece, Italy, Spainand othersin Latin America.

talasemia Specific binding was maximal in the presence of 25 mM phosphate and at pH 5. Thalassemia can be diagnosed via a complete blood counthemoglobin electrophoresis, and DNA testing. Current Opinion in Obstetrics and Gynecology.