Literature DB >> 8099835

Congenital factor VII deficiency complicated with hemoperitoneum and intracranial hemorrhage: report of a case.

Y C Horng1, Y H Chou, R L Chen, K I Tsou, K H Lin.   

Abstract

Hypoproconvertinemia, or factor VII deficiency, is a rare congenital coagulopathy. We report on a female infant with congenital factor VII deficiency complicated by hemoperitoneum and intracranial hemorrhage. Most reports indicate that the bleeding of victims tends to be mild and confined to the superficial mucosa area. However, other reports and our experience with this patient suggest that it can result in fatal cerebral hemorrhage and necessitate early diagnosis, effective treatment and careful genetic counseling.

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Year:  1993        PMID: 8099835

Source DB:  PubMed          Journal:  J Formos Med Assoc        ISSN: 0929-6646            Impact factor:   3.282


  2 in total

1.  Management of Pregnancy in a Chilean Patient with Congenital Deficiency of Factor VII and Glanzmann's Thrombasthenia Variant.

Authors:  Nigel P Murray; Claudio Garcia; Javier Ilabaca; Nestor Lagos
Journal:  Case Rep Obstet Gynecol       Date:  2014-12-01

2.  Novel IVS7+1G>T mutation of life-threatening congenital factor VII deficiency in neonates: A retrospective study in China.

Authors:  Juan He; Wei Zhou; Hui Lv; Li Tao; XiaoWen Chen; Ling Wang
Journal:  Medicine (Baltimore)       Date:  2019-10       Impact factor: 1.889

  2 in total

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