DefinitionThis section has been translated automatically.
Dysprothrombinaemia is an extremely rare, hereditary disease that has been described in less than 20 families. In contrast to hypoprothrombinaemia, normal concentrations of prothrombin are detectable here, but the activity is extremely weakened.
Occurrence/EpidemiologyThis section has been translated automatically.
The inheritance is autosomal recessive.
Clinical featuresThis section has been translated automatically.
Clinically - similar to hypoprothrombinemia - slight bleeding and epistaxis are observed.
LiteratureThis section has been translated automatically.
- HA Neumann (2014) The coagulation system. ABW-Wissenschaftsverlag GmbH Berlin p. 171.
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Hypoprothrombinaemia;Disclaimer
Please ask your physician for a reliable diagnosis. This website is only meant as a reference.
Prof. Dr. med. Peter Altmeyer