CRH: Hereditary Combined Deficiency of the Vitamin K-Dependent Coagulation Factors
CRH French Reference Center for Hemophilia, Lyon shared an insightful post on LinkedIn:
”New publication alert from CRH in Lyon!
CRH in Lyon is involved not only in hemophilia care but also in the management of very rare bleeding disorders.
Hereditary combined vitamin K-dependent coagulation factor deficiency (VKCFD) is an extremely rare genetic disorder with life-threatening bleeding episodes and a range of non-hemostatic issues.
From neonatal bleeding to cardiovascular abnormalities, VKCFD presents unique challenges.
This comprehensive review covers all 57 documented cases of VKCFD, including 4 new, unpublished cases from France.”
Read the full article here.
Article: Hereditary Combined Deficiency of the Vitamin K-Dependent Coagulation Factors
Authors: Alexandre Raharimanana, Séverine Cunat, Céline Falaise, Caroline Oudot, Alexandra Fournel, Yesim Dargaud
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