Combined deficiency of factor V and factor VIII in a pediatric patient: a case report
Our study highlights a rare and often underdiagnosed genetic disorder that is often confused with a diagnosis of minor hemophilia A or congenital factor V deficiency. Differential diagnosis is crucial, particularly for von Willebrand disease. Combined deficiency of factors V and VIII should be suspected in patients with a suggestive clinical and laboratory profile, including prolonged prothrombin time and activated partial thromboplastin time along with a deficiency in coagulation factor V. Therefore, measuring factor VIII levels is highly recommended.
Authors
- Yasmine Bendarkawi (ORCID: https://orcid.org/0000-0002-8860-1542)
- Zakia Berchane
- Azlarab Masrar
- Hassane Mamad (ORCID: https://orcid.org/0000-0001-7170-1021)
- Souad Benkirane
Institutions
- Mohammed V University (MA)
- Centre Hospitalier Ibn Sina (MA)
Publication Details
- Journal
- Journal of Medical Case Reports
- Published
- 2025-04-28
- DOI
- https://doi.org/10.1186/s13256-025-05251-w
- Primary Topic
- Blood properties and coagulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00