Zusammenfassung
Ein 11 Monate altes arabisches Mädchen, 6. Kind blutsverwandter Eltern, kam zur stationären Aufnahme. Im 7. Lebensmonat fielen erstmals rezidivierende Ekchymo-sen auf, im 9. Lebensmonat dann eine 10 × 10 cm große Hautnekrose an der linken Flanke. Das Kind wurde zunächst in die Universitätsklinik Charlottenburg in Berlin, dann in unsere Klinik verlegt. Unabhängig voneinander wurde die Diagnose „homozygoter Protein C-Mangel“ gestellt.
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© 1988 Springer-Verlag Berlin Heidelberg
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Auberger, K. et al. (1988). Substitutionstherapie mit hochgereinigtem Protein C-Konzentrat bei einem Kind mit homozygotem Protein C-Mangel. In: Landbeck, G., Marx, R. (eds) 17. Hämophilie-Symposion. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-72830-3_85
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DOI: https://doi.org/10.1007/978-3-642-72830-3_85
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