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Indian J Pediatr ; 81(3): 283-4, 2014 Mar.
Article in English | MEDLINE | ID: mdl-23881482

ABSTRACT

Congenital factor V deficiency (also known as labile factor or proaccelerin) is a rather uncommon [1:1000,000] inherited coagulopathy (autosomal recessive inheritance). Affected patients become symptomatic in early childhood with spontaneous or post-traumatic bleeding complications. The authors report an infant who presented with a much feared complication of the same probably as a neonatal presentation.


Subject(s)
Factor V Deficiency/complications , Blood Coagulation Factors/analysis , Factor V Deficiency/blood , Humans , Infant , Male
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