Inherited protein-C deficiency, factor V G 1691 A and FV A 4070 G mutations in a child with internal cerebral venous thrombosis.

Abstract:

:Common systemic disorders that cause cerebral venous thrombosis (CVT) in children include dehydration, trauma, infection and haematological diseases. No cause for CVT is identified in one quarter of all cases. We report a child with thalamic infarcts due to internal CVT who had congenital heterozygous protein-C deficiency, factor V G 1691 A and A 4070 G mutations.

journal_name

Pediatr Radiol

journal_title

Pediatric radiology

authors

Sipahi T,Uner C,Yildiz YT,Akar N

doi

10.1007/s002470050776

keywords:

subject

Has Abstract

pub_date

2000-06-01 00:00:00

pages

420-3

issue

6

eissn

0301-0449

issn

1432-1998

journal_volume

30

pub_type

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