A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW

A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW

Factor 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 inhe...

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Bibliographic Details
Main Author: Zuhair Al-Barazanchi
Format: Article
Language:English
Published: university of basrah 2006-06-01
Series:Basrah Journal of Surgery
Subjects:
factor xiii
deficiency
Online Access:https://bjsrg.uobasrah.edu.iq/article_55343_1d914d154fbab23603c0ec86189bba70.pdf
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spelling doaj-539a196c6d024c6b8d91cde404b4a02e2020-11-25T03:05:36Zenguniversity of basrahBasrah Journal of Surgery1683-35892409-501X2006-06-011210010.33762/bsurg.2006.5534355343A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEWZuhair Al-BarazanchiFactor 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.https://bjsrg.uobasrah.edu.iq/article_55343_1d914d154fbab23603c0ec86189bba70.pdffactor xiiideficiency
collection DOAJ
language English
format Article
sources DOAJ
author Zuhair Al-Barazanchi
spellingShingle Zuhair Al-Barazanchi
A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW
Basrah Journal of Surgery
factor xiii
deficiency
author_facet Zuhair Al-Barazanchi
author_sort Zuhair Al-Barazanchi
title A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW
title_short A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW
title_full A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW
title_fullStr A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW
title_full_unstemmed A FAMILY WITH FACTOR XIII DEFICIENCY CASE REPORT AND LITERATURE REVIEW
title_sort family with factor xiii deficiency case report and literature review
publisher university of basrah
series Basrah Journal of Surgery
issn 1683-3589
2409-501X
publishDate 2006-06-01
description Factor 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.
topic factor xiii
deficiency
url https://bjsrg.uobasrah.edu.iq/article_55343_1d914d154fbab23603c0ec86189bba70.pdf
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AT zuhairalbarazanchi familywithfactorxiiideficiencycasereportandliteraturereview
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