Dysfibrinogenesis D68.-

Author: Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 29.10.2020

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Definition
This section has been translated automatically.

A rare cause of hereditary thrombophilia is the genetic variation of the fibrin molecule. This genetic disposition has only been described in about 300 families. Often this mutation is not symptomatic.

Literature
This section has been translated automatically.

  1. HA Neumann (2014) The coagulation system. ABW-Wissenschaftsverlag GmbH Berlin S. 232.

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Outgoing links (1)

Thrombophilia, hereditary;

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Please ask your physician for a reliable diagnosis. This website is only meant as a reference.

Authors

Last updated on: 29.10.2020

Author: Prof. Dr. med. Peter Altmeyer Prof. Dr. med. Peter Altmeyer

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