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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Blood tests, genetic tests [3]. Mosby Elsevier, Rapid Review Series. Archived from the original on 16 September Data Keadaan Fisik Anak Thalasemia a.

A screening policy exists in Cyprus to reduce the rate of thalassemia, which, since the program’s implementation in the s which also tyalasemia prenatal screening and abortionhas reduced the number of children born with the disease from one of every births to almost zero.

It has the benefit of being inexpensive and decent long-term safety. Thalassemias are genetic disorders inherited from a person’s parents.

While one person with beta thalassemia has no longer required blood transfusions following treatment within a research trial, it is not an approved treatment as of Remember me Forgot password? Iron-deficiency anemia Plummer—Vinson syndrome Macro-: Department of Medical Sciences. A large peak of 40 s duration was followed by another, however smaller, transient rise of comparable duration.


In Europe, the highest concentrations of the disease are found in Greececoastal regions in Turkey askel the Aegean Region such as IzmirBalikesirAydinMuglaand Mediterranean Region such as AntalyaAdanaMersinin parts of Italyparticularly southern Italy and the lower Po valley. Beta thalassemias are due to mutations in the HBB gene on chromosome 11, [24] also inherited in an autosomal, recessive fashion.

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Thalassemias are particularly associated with people of Mediterranean origin, Arabs especially Palestinians and people of Palestinian descentand Asians. Estimates suggest that approximately 1. A blood transfusion regimen was the first measure effective in prolonging life.

Implementasi Implementasi yang dilakukan sesuai intervensi keperawatan E.

Inin Spain, a baby was selectively implanted to be a cure for his brother’s thalassemia. Archived from the original on 28 July Nowadays, it is found in populations living in Africa, the Americas, and in Tharu people in the Terai region of Nepal and India.


Help Center Find new research papers in: The cost is also significant. Current Opinion in Obstetrics and Gynecology.


Analysis of clinical evidences and their relations. Askep Nanda,Noc,Nic Thypoid askep nanda,noc,nic thypoid.

Specific binding was maximal in the presence of 25 mM phosphate and at pH 5. Other Mediterranean people, as well as those in the vicinity of the Mediterranean, also have high rates of thalassemia, including people from West Asia and North Africa.

Kerusakan integritas kulit tidak terjadi.

Askep Teori Thalasemia Nic Noc

Feeling tiredpale skinenlarged spleenyellowish skindark urine [1]. Retrieved 24 February Pola Makan Karena adanya anoreksia sehingga anak sering mengalami susah makan.

Adverse effects are primary skin reactions around the injection site and hearing loss. This potentially results in a progressive increase in hemoglobin A2 synthesis in all subsequent developing red blood cells, with resultant thalsaemia of the anemia.

Askep Teori Thalasemia Nic Noc – PDF Free Download

Thalassemias also asmep in descendants of people from Mediterranean countries e. Terlihat pucat, dipalpasi ada pembesaran limpa dan hati hepatospek nomegali. American Journal of Human Genetics.