ParahaemophiliaD68.2

Author:Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 29.10.2020

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Synonym(s)

congenital factor V deficiency; Factor V deficiency congenital; Hypoproaczeleremia; Owen's disease

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HistoryThis section has been translated automatically.

Owren, 1947

DefinitionThis section has been translated automatically.

Autosomal recessive inherited factor V deficiency with a tendency to bleed.

ManifestationThis section has been translated automatically.

Early childhood.

Clinical featuresThis section has been translated automatically.

Bleeding of the nose, gums, ecchymosis, suffusions, menorrhages, gastrointestinal bleeding, cerebral bleeding, combination with other malformations possible.

LaboratoryThis section has been translated automatically.

Extended prothrombin time.

DiagnosisThis section has been translated automatically.

Proof of factor V deficiency.

TherapyThis section has been translated automatically.

Fresh whole blood, fresh plasma.

Progression/forecastThis section has been translated automatically.

Awkward.

LiteratureThis section has been translated automatically.

  1. Owren P (1947) Parahaemophilia: haemorrhagic diathesis due to absence of a previously unknown clotting factor. Lancet I: 446-448

Authors

Last updated on: 29.10.2020

Author: Prof. Dr. med. Peter Altmeyer