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Article

Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 May 2009

Landau D, Rosenberg N, Zivelin A, Staretz-Chacham O, Kapelushnik J

Abstract excerpt

Inherited factor VII (FVII) deficiency is a rare autosomal recessive disorder with a wide heterogeneous clinical pattern. Intracranial haemorrhage in infants has been previously reported in the severe form of the FVII deficiency and it has a high fatality rate. We report a family with high consanguineous relations, who experienced death of two baby girls, the first with prenatal manifestation of foetal...

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Identifiers

PMID: 19432927
DOI: 10.1111/j.1365-2516.2009.02004.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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