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Factor I deficiency
- ... found to cause a rare bleeding disorder called factor X deficiency. This disorder commonly causes nosebleeds, easy bruising, bleeding ... or trauma. Some F10 gene mutations that cause factor X deficiency reduce the amount of coagulation factor X in ...
- ... found to cause a rare bleeding disorder called factor VII deficiency. This disorder commonly causes nosebleeds, easy bruising, bleeding ... A, De Bosch N, Salazar-Sanchez L; Greifswald Factor FVII Deficiency Study Group. Factor VII deficiency: clinical manifestation of ...
- ... gene have been identified in people with complement factor I deficiency, a disorder characterized by immune system dysfunction. The ... which may also occur in people with complement factor I deficiency, is characterized by kidney malfunction that can be ...
- ... found to cause a rare bleeding disorder called factor XI deficiency. This disorder, while usually mild, can cause nosebleeds, ... or trauma. The F11 gene mutations that cause factor XI deficiency reduce the amount of factor XI in the ...
- ... gene can also cause a disorder known as factor XII deficiency. Factor XII deficiency is an inherited condition characterized by a shortage ... do not experience abnormal bleeding or other symptoms. Factor XII deficiency is typically discovered during routine blood testing because ...
- ... found to cause a rare bleeding disorder called factor V deficiency. These variants prevent the production of functional coagulation ... episodes of abnormal bleeding that can be severe. Factor V deficiency results from variants in both copies of the ...
- ... F13A1 gene have been found to cause inherited factor XIII deficiency, a rare bleeding disorder. Without treatment, affected individuals ... A, Ivaskevicius V, Thomas A, Oldenburg J. Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired ...
- ... F13B gene have been found to cause inherited factor XIII deficiency, a rare bleeding disorder. Without treatment, affected individuals ... A, Ivaskevicius V, Thomas A, Oldenburg J. Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired ...
- ... M, Zanon E, Girolami A. Severe prekallikrein (Fletcher factor) deficiency due to a compound heterozygosis (383Trp stop codon ...
- ... in the FGA gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
