Familial vitamin K metabolism deficiency responsible for a congenital binder phenotype
A 4-month-old male born with a Binder Phenotype was admitted for the evacuation of a large subdural hematoma. The blood analysis revealed a prolonged prothrombin time due to vitamin K-dependent coagulation factor deficiency. Vitamin K participates in the embryonic development of the nasal cartilage. The genetic analysis of our patient revealed a rare genetic cause, responsible for the congenital Binder phenotype associated with a defect in the vitamin K metabolism, a pathogenic variant in the GGCX gene that has not been previously reported in the literature. All neonates presenting a Binder Phenotype would benefit from coagulation screening, an easy-access exam, in order to prevent severe and potentially dreadful hemorrhagic events.
Authors
- A. Mathonnet (ORCID: https://orcid.org/0000-0002-6924-7947)
- Konstantinos Grammatopoulos
- Nancy Végas (ORCID: https://orcid.org/0000-0002-8293-2383)
- Cristina Peduto (ORCID: https://orcid.org/0000-0003-4054-3651)
- Annie Harroche (ORCID: https://orcid.org/0000-0001-7368-4624)
- Véronique Abadie (ORCID: https://orcid.org/0000-0002-3525-1921)
- Geneviève Baujat (ORCID: https://orcid.org/0000-0001-7435-0298)
- Alix Flamant
Institutions
- Hôpital Necker-Enfants Malades (FR)
- Université Paris Cité (FR)
- Institut Necker Enfants Malades (FR)
- Assistance Publique – Hôpitaux de Paris (FR)
Publication Details
- Journal
- Archives de Pédiatrie
- Published
- 2025-06-24
- DOI
- https://doi.org/10.1016/j.arcped.2025.05.003
- Primary Topic
- Vitamin K Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00