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Bleeding Symptoms in Pediatric Patients with Congenital FVII Deficiency and Correlation to Thrombin...

Bleeding Symptoms in Pediatric Patients with Congenital FVII Deficiency and Correlation to Thrombin...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1fcf9720bc9a40d4b91adfb3ce2b8553

Bleeding Symptoms in Pediatric Patients with Congenital FVII Deficiency and Correlation to Thrombin Generation Assay Parameters: A Single-Center Retrospective Analysis

About this item

Full title

Bleeding Symptoms in Pediatric Patients with Congenital FVII Deficiency and Correlation to Thrombin Generation Assay Parameters: A Single-Center Retrospective Analysis

Publisher

Switzerland: MDPI AG

Journal title

Life (Basel, Switzerland), 2024-12, Vol.14 (12), p.1559

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Inherited factor VII deficiency is the most common rare bleeding disorder, affecting about 1/500,000 individuals without gender predilection. Most of the patients with FVII 20–50% are asymptomatic, but post-traumatic or post-surgical bleeding may often occur since there is not an exact correlation between FVII plasma levels and the bleeding phenoty...

Alternative Titles

Full title

Bleeding Symptoms in Pediatric Patients with Congenital FVII Deficiency and Correlation to Thrombin Generation Assay Parameters: A Single-Center Retrospective Analysis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_1fcf9720bc9a40d4b91adfb3ce2b8553

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1fcf9720bc9a40d4b91adfb3ce2b8553

Other Identifiers

ISSN

2075-1729

E-ISSN

2075-1729

DOI

10.3390/life14121559

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