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International registry on factor XIII deficiency: a basis formed mostly on European data.

Thrombosis and haemostasis - 1 Jun 2007

Ivaskevicius Vytautas, Seitz Rainer, Kohler Hans P, Schroeder Verena, Muszbek Laszlo, Ariens Robert A S, Seifried Erhard, Oldenburg Johannes

Abstract excerpt

FXIII deficiency is known as one of the rarest blood coagulation disorders. In this study, the phenotypic and in part genotypic data of 104 FXIII-deficient patients recorded from 1993 - 2005 are presented. The most common bleeding symptoms were subcutaneous bleeding (57%) followed by delayed umbilical cord bleeding (56%), muscle hematoma (49%), hemorrhage after surgery (40%), hemarthrosis (36%), and intracerebral...

Topics

Abortion, Spontaneous
Adult
Blood Coagulation
Coagulants
Europe
Factor XIII
Factor XIII Deficiency
Female
Founder Effect
Genotype
Haplotypes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Hemorrhage

Humans

International Cooperation

Internet

Male

Mutation

Pedigree

Source

Identifiers

PMID: 17549292

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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