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Article

Factor X deficiency and intracranial bleeding: who is at risk?

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Sept 2011

Rauch R, Girisch M, Wiegand G, Schroeder W, Hofbeck M, Welisch E, Wulff K

Abstract excerpt

Very few mutations of the gene encoding for coagulation factor X (FX) have been found associated with intracranial haemorrhage (ICH) due to FX deficiency (FXD). No guidelines exist as to when prophylaxis in FXD should be started and how patients at risk for ICH can be identified. We report on a n...

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PMID: 21682820
DOI: 10.1111/j.1365-2516.2011.02591.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21682820-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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