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Sickle Cell Disease Patient
Macmillan Education (Verlag)
978-0-333-39239-3 (ISBN)
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An approach to treatment is given, with greater emphasis on patient management than is usual, paying attention to aggravating factors such as infections within poor socio-economic conditions and stressing the importance of genetic counselling and family planning for patients.
Part 1 Historical survey and review of the literature: historical observations; sickle cell disease in successive Ghanaian generations for 3 centuries; some general observations on the genetic expression of sickle cell disease; sickle cell disease as an haemoglobinopathy; the molecular pathology of sickle cell haemoglobin and other haemoglobin variants; genetic control of haemoglobin synthesis. Part 2 Clinical features 1: history of sickle cell disease in the world; balanced polymorphism and other factors relating to hereditary qualitative and quantitative erythrocyte defects; the pathgenesis of sickle cell disease; the crisis in sickle cell disease. Part 3 Clinical features 2: patients and methods, the sickle cell/haemoglobinopathy clinic of Korle Bu teaching hospital; rheumatism, dactylitis and seasonal epidemiology of sickle cell crises in Accra; pallor and jaundice in sickle cell disease; gnathopathy, bossing of skull bones and finger clubbing in sickle cell disease; body habitus and growth in sickle cell disease; sickle cell dermathopathy in Accra; epistaxis and haematuria - two bleeding tendencies in sickle cell states; sickle cell ophthalmopathy; sickle cell priapism; articular bone neurosis in scikle cell disease; skeletal involvement in sickle cell disease; abdominal pain in sickle cell disease; the liver in sickle cell disease; the spleen and lymphnodes in sickle cell disease; cardio-respiratory involvement in sickle cell disease; sickle cell disease and the central nervous system; some quantitative aspects of pregnancy in sickle cell disease in Accra; notes on some miscellaneous clinical features of sickle cell disease. Part 4 Some laboratory and other findings in sickle cell disease: haemotological profile in sickle cell disease; percentage values of haemoglobins S,F,A2,C and A is various sickle cell phenotypes and the position of the sickle cell trait; some aspects of renal function in sickle cell disease; some radio-active isotope patterns of sickle cell disease in Accra. Part 5 Management and conclusions: an approach to the treatment of sickle cell disease; the prognostic and public health aspects of sickle cell disease in Accra; the socio-politics of "Sickle Cell"; conclusions - the whole person. Appendices: Case histories; some laboratory investigations; Korle Bu hospital schedule for emergency treatment of sickle cell crisis; list of some sickle cell disease patient orientated centres in the world.
Erscheint lt. Verlag | 20.3.1991 |
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Verlagsort | London |
Sprache | englisch |
Maße | 189 x 246 mm |
Gewicht | 1267 g |
Themenwelt | Medizinische Fachgebiete ► Innere Medizin ► Hämatologie |
Studium ► 1. Studienabschnitt (Vorklinik) ► Histologie / Embryologie | |
ISBN-10 | 0-333-39239-6 / 0333392396 |
ISBN-13 | 978-0-333-39239-3 / 9780333392393 |
Zustand | Neuware |
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