Catalog

Hereditary factor XIII deficiency

No MMS code

Link to WHO Definition

Hereditary factor XIII deficiency – http://id.who.int/icd/entity/2079957863

Congenital factor XIII deficiency is an inherited bleeding disorder due to reduced levels and activity of factor XIII and characterised by haemorrhagic diathesis frequently associated with spontaneous abortions and defective wound healing. Factor XIII deficiency is one of the most rare coagulation factor deficiencies. Both sexes are equally affected.