A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW | Zendy

Zuhair Al-Barazanchi | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Open Access

A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW

Author(s) -

Zuhair Al-Barazanchi

Publication year - 2006

Publication title -

basrah journal of surgery

Language(s) - English

Resource type - Journals

eISSN - 2409-501X

pISSN - 1683-3589

DOI - 10.33762/bsurg.2006.55343

Subject(s) - factor xiii deficiency , factor xiii , girl , coagulation , medicine , coagulation disorder , pediatrics , surgery , genetics , biology , fibrinogen

actor XIII deficiency is a rare disorder of coagulation characteri-zed by moderate to severe bleeding tendency with increased susceptibility to intracranial hemorrhages, almost normal coagulation screening tests, clot lysis in 5 M urea solution & a tendency to abnormal wound healing. It is inherited as an autosomal recessive trait. However, acquired causes for its deficiency are rarely encountered. We describe here an inherited form of F XIII deficiency in two members (a boy & a girl) in a one family in Basrah. F

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research