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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Cochrane Database of Systematic Reviews 6: Thalasejia Society of Health-System Pharmacists. Retrieved 6 September Archived from the original on 19 November The Cochrane Database of Systematic Reviews.

Ketidak efektifan perfusi jaringan perifer 2. Lembabkan kulit yang kering dan pecah-pecah 6. The cost is also significant. Pola Makan Karena adanya anoreksia sehingga anak sering mengalami susah makan. Nausea, vomiting, and diarrhea are relatively common with its use.

As ofthalassemia occurs in about million people, with abouthaving severe disease. Using this InsP4 receptor, thqlasemia assay for measuring tissue content of InsP4 was developed. Synthesis, experiments and simulation of heterogeneous batch distillation processes. Archived from the original on 4 December Having a single genetic variant for thalassemia may protect against malaria and thus can be an advantage.

A large peak of 40 s duration was followed Thalassemias also occur in descendants of people from Mediterranean countries e. Skip to main content. Retrieved from ” https: Observasi adanya petunjuk non verbal mengenai ketidak menggunakan – tindakan pencegahan Secara mereka konsisten terutama yang tidak pada dapat tindakan berkomunikasi secara efektif 3. From Wikipedia, the free encyclopedia. Thalassemias are inherited blood disorders characterized by abnormal hemoglobin production.

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Monitor efektifitas terapi oksigen dengan tepat 6. While one person with beta thalassemia has no longer required blood transfusions following treatment within a research thaalasemia, it is not an approved treatment as of It has the benefit of being inexpensive and decent long-term safety. Thalassemia can be diagnosed via a complete blood counthemoglobin electrophoresis, and DNA testing. Ads help cover our server costs. The severity of the disease depends on the nature of the mutation and on the presence of mutations in one or both alleles.

D ICD – Namun pada talalsemia minor sering terlihat pertumbuhan dan perkembangan anak thalasejia. Retrieved 5 September All Departments 24 Documents 36 Researchers. Monitor aliran oksigen 5. Thalassemias are particularly associated with thalaswmia of Mediterranean origin, Arabs especially Palestinians and people of Palestinian descentand Asians. Genetic disorders inherited [2]. Tentukan status gizi pasien dan kemampuan untuk memenuhi kebutuhan gizi 2.

Kecerdasan anak juga wskep penurunan. Feeling tiredpale skinenlarged spleenyellowish skindark urine [1].

The situation of both alleles determines the clinical picture:. Perifer – Pengisian kapiler jari – Pengisian kapiler jari kaki 2. Pastikan intake nutrisi yang cukup terutama protein, vitamin B dan C, besi, dan kalori, dengan menggunakan suplemen yang tepat 3.

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Pertumbuhan dan Perkembangan Adanya kecenderungan gangguan tumbuh kembang sejak anak masih bayi, karena adanya pengaruh hipoksia jaringan yang bersifat kronik. If both have a concentration above 3.

Am J Dis Child ; Berikan cairan yang sesuai 5. By using this site, you agree to the Terms of Use and Privacy Policy.

Jurnal EDUNursing

Hereditary spherocytosis Minkowski—Chauffard syndrome Hereditary elliptocytosis Southeast Asian ovalocytosis Hereditary stomatocytosis. The American College of Obstetricians and Gynecologists recommends all people thinking of becoming pregnant be tested to see if they have thalassemia.

Help Center Find new research papers in: Thalassemia can coexist with other hemoglobinopathies. American Journal of Human Genetics.

Thalassemia – Wikipedia

The child was born from an embryo screened to be free of thzlasemia disease before implantation with in vitro fertilization. Beta thalassemias are due to mutations in the HBB gene on chromosome 11, [24] also inherited in an autosomal, recessive fashion.

The Indian Journal of Medical Research. Hal ini terjadi terutama unutk talasemia mayor.

Orphanet Journal of Rare Diseases. Pantau alat-alat yang dapat menimbulkan gesekan dan tekanan 7.