Research Evidence
Peer-reviewed studies linked via MeSH term "von Willebrand Disease, Type 2" from the MEDLINE/PubMed database.
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Laboratory assays of VWF activity and use of desmopressin trials in the diagnosis of VWD: a systematic review and meta-analysis.
[object Object], [object Object], [object Object] et al. · Blood Adv · 2022
Type 2B von Willebrand Disease in Pregnancy: A Systematic Literature Review.
[object Object], [object Object], [object Object] et al. · Semin Thromb Hemost · 2021
PMID: 33636751Meta-Analysis
A randomised pilot trial of the anti-von Willebrand factor aptamer ARC1779 in patients with type 2b von Willebrand disease.
[object Object], [object Object], [object Object] et al. · Thromb Haemost · 2010
PMID: 20589313RCT
Von Willebrand Factor Multimer Analysis and Classification: A Comprehensive Review and Updates.
[object Object], [object Object], [object Object] et al. · Semin Thromb Hemost · 2023
PMID: 36174612Review
Von Willebrand disease type 2N: An update.
[object Object], [object Object], [object Object] · J Thromb Haemost · 2021
PMID: 33497541Review
How I manage severe von Willebrand disease.
[object Object], [object Object] · Br J Haematol · 2019
How I treat type 2B von Willebrand disease.
[object Object], [object Object] · Blood · 2018
PMID: 29378695Review
Diagnostic Differentiation of von Willebrand Disease Types 1 and 2 by von Willebrand Factor Multimer Analysis and DDAVP Challenge Test.
[object Object], [object Object], [object Object] et al. · Clin Appl Thromb Hemost · 2017
PMID: 27443694Review
Advances in the diagnosis and treatment of Von Willebrand disease.
[object Object], [object Object] · Hematology Am Soc Hematol Educ Program · 2017
Diagnosing von Willebrand disease: genetic analysis.
[object Object] · Hematology Am Soc Hematol Educ Program · 2016
Search all PubMed articles for von Willebrand disease type 2
Research data from MEDLINE/PubMed
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Bruising susceptibility
HP:0000978
Frequent nosebleeds
HP:0000421
Hypermenorrhea
HP:0000132
Low platelet count
HP:0001873
Quick Facts
- SNOMED CT
- 128107007
- UMLS CUI
- C1264040
- Fully Specified Name
- Hereditary von Willebrand disease type 2 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 4
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.