Súlyos hereditaer V. factor-hiányos beteg esetének ismertetese.

Marosi Anikó, Apjok Eniko, Magyarosy Edina, Szabó Teréz, Ajzner Eva

Research output: Article


Introduction: Congential deficiency of factor V is a rare condition, transmitted in autosomal recessive way. Heterozygote patients generally have no symptoms, homozygotes present with spontaneous and postoperative bleedings. About one-half of patients are diagnosed in adulthood. Methods: The presented case is a double heterozygote, which was confirmed using moleculare biological methods. The authors found many carriers in his family. Conclusions: This rare and sometimes severe disorder needs regular haematological controls. Carriers must have more attention during surgical procedures and labour, and the family doctor should be informed about there condition.

Original languageHungarian
Pages (from-to)87-89
Number of pages3
JournalOrvosi hetilap
Issue number2
Publication statusPublished - jan. 13 2002


ASJC Scopus subject areas

  • Medicine(all)

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