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

[Combined deficiency of clotting factor V and factor VIII: about three siblings].

The Pan African medical journal - 1 Jan 2021

Mamad Hassane, Benkirane Souad, Aissaoui Yousra El, Berchane Zakia, Masrar Azlarab

Abstract excerpt

Combined deficiency of clotting factor V and factor VIII (DF5F8) is a congenital autosomal recessive disorder. This study involved a family of four children born to consanguineous parents. The eldest daughter was referred for assessment of activated partial thromboplastin time and prothrombin time associated with hemorrhagic manifestations. Coagulation factor dosing showed combined deficiency of factor V and...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child, Preschool
Share to Factor V Deficiency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemophilia A

Share to Mannose-Binding Lectins

Share to Membrane Proteins

Share to Siblings

Share to Vesicular Transport Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 34422188
DOI: 10.11604/pamj.2021.39.65.24559
PMCID: PMC8363970

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

[Combined deficiency of clotting factor V and factor VIII: about three siblings].PMID 34422188Read ↗

Combined Factor V and VIII Deficiency with LMAN1 Mutation: A Report of 3 Saudi Siblings.Semantic proximity Read ↗

[Combined deficiency of factors V and VIII caused by a novel compound heterozygous mutation of gene Lman1].Semantic proximity Read ↗

Combined FV and FVIII deficiency.Semantic proximity Read ↗

Combined Factor V and Factor VIII Deficiency.Semantic proximity Read ↗

Combined deficiency of coagulation factors V and VIII: an update.Semantic proximity Read ↗

Inherited and acquired factor V deficiency.Semantic proximity Read ↗

Genotype and phenotype report on patients with combined deficiency of factor V and factor VIII in Iran.Semantic proximity Read ↗

Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.Semantic proximity Read ↗

Recent developments in the understanding of the combined deficiency of FV and FVIII.Semantic proximity Read ↗

A new case of combined factor V and factor VIII deficiency further suggests that the LMAN1 M1T mutation is a frequent cause in Italian patients.Semantic proximity Read ↗

Combined factor V and factor VIII deficiency in a Thai patient: a case report of genotype and phenotype characteristics.Semantic proximity Read ↗

Analysis of newly detected mutations in the MCFD2 gene giving rise to combined deficiency of coagulation factors V and VIII.Semantic proximity Read ↗

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