Hereditary hypofibrinogenemia: A rare cause of chronic liver disease
Hypofibrinogenemia is characterized by low levels of fibrinogen with patients commonly presenting asymptomatically. This report discusses a case of hereditary hypofibrinogenemia manifesting as chronic liver disease in a 2-year-old male who was evaluated for elevated liver enzymes and skin/soft tissue bleeding.
Authors
- Akshat Jain (ORCID: https://orcid.org/0000-0001-6433-7997)
- Kalyan Ray Parashette
- Khyati Mehta
- Nolan Maloney (ORCID: https://orcid.org/0000-0002-4088-6497)
- Hannah Caringal
Institutions
- Loma Linda University Children's Hospital (US)
Publication Details
- Journal
- JPGN Reports
- Published
- 2025-06-27
- DOI
- https://doi.org/10.1002/jpr3.70058
- Primary Topic
- Blood properties and coagulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00