Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories.

International journal of laboratory hematology - 1 Dec 2017

Jennings I, Kitchen S, Menegatti M, Palla R, Walker I, Peyvandi F, Makris M

Abstract excerpt

INTRODUCTION: Mutations in fibrinogen (Fgn) genes, causing dysfibrinogenaemia, can result in either a bleeding or thrombophilic diathesis. Dysfibrinogenaemia is infrequently encountered in hospital laboratories, and the utility of different assays in the diagnosis of dysfibrinogenaemia has not previously been explored in a multicentre study. We describe here an exercise in which PRO-RBDD project (prospective data...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Afibrinogenemia
Share to Blood Coagulation Tests

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diagnostic Errors

Share to Fibrinogen

Share to Mutation

Share to United Kingdom

Source

Identifiers

PMID: 28766854
DOI: 10.1111/ijlh.12721

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories.PMID 28766854Read ↗

Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias.Semantic proximity Read ↗

Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia.Semantic proximity Read ↗

Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.Semantic proximity Read ↗

Can the phenotype of inherited fibrinogen disorders be predicted?Semantic proximity Read ↗

Laboratory diagnosis of dysfibrinogenemia.Semantic proximity Read ↗

p.Tyr365Cys change in factor VIII: haemophilia A, but not as we know it.Semantic proximity Read ↗

Multilaboratory testing in thrombophilia through the United Kingdom National External Quality Assessment Scheme (Blood Coagulation) Quality Assurance Program.Semantic proximity Read ↗

Fibrinogen Magdeburg I: a novel variant of human fibrinogen with an amino acid exchange in the fibrinopeptide A (Aalpha 9, Leu-->Pro).Semantic proximity Read ↗

Novel fibrinogen mutation γ314Thr→Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia.Semantic proximity Read ↗

Unusual A alpha 16Arg-->Cys dysfibrinogenaemic family: absence of normal A alpha-chains in fibrinogen from two of four heterozygous siblings.Semantic proximity Read ↗

Recent progress in the pathophysiology of fibrinogen.Semantic proximity Read ↗

Automated screening procedure for the phenotypes of congenital fibrinogen disorders using novel parameters, |min1|c and Ac/|min1|c, obtained from clot waveform analysis using the Clauss method.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.