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

Co-inheritance of mild hemophilia A and heterozygosity for type 2N von Willebrand disease: a diagnostic and therapeutic challenge.

Pediatric blood & cancer - 1 Oct 2014

Lindsay Holly, Bergstrom Katie, Srivaths Lakshmi

Abstract excerpt

Hemophilia A and von Willebrand disease are the two most common inherited bleeding disorders. Despite their frequency, however, there are very few reports of co-inheritance of the two disorders. We present the first report of a patient with mild hemophilia A and heterozygosity for type 2N von Willebrand disease (VWD). We discuss the patient's phenotype and highlight the diagnostic and therapeutic challenges...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to Factor VIII
Share to Hemophilia A

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Heterozygote

Share to Phenotype

Share to von Willebrand Disease, Type 2

Share to von Willebrand Factor

Source

Identifiers

PMID: 24706524
DOI: 10.1002/pbc.25054

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Co-inheritance of mild hemophilia A and heterozygosity for type 2N von Willebrand disease: a diagnostic and therapeutic challenge.PMID 24706524Read ↗

A diagnostic approach to mild bleeding disorders.Semantic proximity Read ↗

The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory Network.Semantic proximity Read ↗

The molecular analysis of haemophilia A: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network.Semantic proximity Read ↗

von Willebrand disease: Diagnosis and treatment, treatment of women, and genomic approach to diagnosis.Semantic proximity Read ↗

von Willebrand disease update: diagnostic and treatment dilemmas.Semantic proximity Read ↗

Mild hemophilia A.Semantic proximity Read ↗

Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders.Semantic proximity Read ↗

Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice.Semantic proximity Read ↗

The molecular analysis of haemophilia B: a guideline from the UK haemophilia centre doctors' organization haemophilia genetics laboratory network.Semantic proximity Read ↗

Congenital von Willebrand disease type I: definition, phenotypes, clinical and laboratory assessment.Semantic proximity Read ↗

Making a diagnosis of VWD.Semantic proximity Read ↗

The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource.Semantic proximity Read ↗

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