| Literature DB >> 19409767 |
L Sfaihi Ben Mansour1, A Thabet, H Aloulou, H Turki, I Chabchoub, F Mhiri, Z Mnif, H Ben Ali, T Kammoun, M Hachicha.
Abstract
Constitutional factor VII deficiency is a hereditary disease with recessive autosomic transmission. Its incidence is estimated to be 1/1,000,000 in the general population. We report a case of severe factor VII deficiency in infancy revealed by an intracranial hemorrhage in a 2-month-old infant. We describe the clinical, biological and therapeutic characteristics of this disease.Entities:
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Year: 2009 PMID： 19409767 DOI： 10.1016/j.arcped.2009.03.009
Source DB: PubMed Journal: Arch Pediatr ISSN： 0929-693X Impact factor: 1.180