CareLit · DOI-Nachweis · Zeitschrift für Orthopädie und Unfallchirurgie
Severe prekallikrein deficiency due to a compound heterozygosis in the KLKB1-gene
DOI 10.1055/s-0037-1617022
Bibliografische Angaben
Nachweis in CareLit
Autor:innenKochhan, L.; Heuchel, P.; Jenderny, J.; Maak, B.
ZeitschriftZeitschrift für Orthopädie und Unfallchirurgie
Ausgabe02/2009
Jahrgang / SeitenJg. 29 · S. 187 bis 189
Kernaussage aus der Literatur
Abstract-Vorschau
SummaryA 14 year old boy was referred to us for a detailed coagulation study because a previously performed aPTT has been found prolonged. The boy had no history of bleeding symptoms and also the family history was negative for bleeding or thrombotic events. The aPTT in the patient was 96 s (reference range: 24–36 s), prothrombin time and thrombin time were both normal.As the cause for the prolonged aPTT we identifi…
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Zitierempfehlung
Kochhan, L.; Heuchel, P.; Jenderny, J.; Maak, B (2009) Severe prekallikrein deficiency due to a compound heterozygosis in the KLKB1-gene. Zeitschrift für Orthopädie und Unfallchirurgie, 29 (02), 187 bis 189. https://doi.org/10.1055/s-0037-1617022
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