Article

A child with FactorⅤdeficiency misdiagnosed as a left iliac fossa abscess having novel F5 gene mutation: a case report

2022-12-19

Abstract excerpt

<h4>Background: </h4> Congenital FⅤdeficiency is identified as a rare bleeding disorder (RBD) that is expressed in an autosomal recessive manner and generally occurs in one part per million of the population.This disorder is accompanied by a variety of clinical manifestations. The factorⅤgene variant c.2439delC (p.I814Lfs*23 ) in exon 13 was first reported in this case. Case presentation： A 13-year-old male patie...

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Literature Corpus work: 18f9e2cd-38cd-5d2f-9e0b-24c56a2454f2
DOI: 10.21203/rs.3.rs-2342675/v1

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