Afibrinogenemia with two compound heterozygous mutations in FGA gene
Haemophilia
.
2021 Sep;27(5):e641-e644.
doi: 10.1111/hae.14377.
Epub 2021 Jul 13.
Authors
Guillaume Feugray
1
,
Paul Billoir
1
,
Alessandro Casini
2
,
M Neerman-Arbez
3
,
Virginie Barbay
1
4
,
Pierre Chamouni
4
,
Pascale Schneider
5
,
Véronique Le Cam Duchez
1
4
Affiliations
1
UNIROUEN, INSERM U1096, Vascular Hemostasis Unit, Normandie University, Rouen University Hospital, France.
2
Division of Angiology and Hemostasis, Faculty of Medicine, Geneva University Hospitals, Geneva, Switzerland.
3
Department of Genetic Medicine and Development, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
4
Hemophilia Care Center, Rouen University Hospital, Rouen, France.
5
Department of Pediatric Hematology and Oncology, Rouen University Hospital, Rouen, France.
PMID:
34255402
DOI:
10.1111/hae.14377
No abstract available
Keywords:
bleeding; cephalhaematoma; hereditary afibrinogenemia.
Publication types
Letter
MeSH terms
Afibrinogenemia* / diagnosis
Afibrinogenemia* / genetics
Fibrinogen / genetics
Humans
Mutation
Substances
FGA protein, human
Fibrinogen