HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

[Congenital factor XIII deficiency in pregnancy. A case report].

Abstract
Congenital factor XIII deficiency is a rare hemorrhagic syndrome with an altered fibrin stability, hemorrhagic diathesis and habitual abortions. After a short introduction, a case report is described and the clinical differences between plasmatic and platelet deficiency pointed out.
AuthorsG Cerenzia, L Serrao, C Carillo, M R Manna, V S Niccoli
JournalMinerva ginecologica (Minerva Ginecol) Vol. 51 Issue 10 Pg. 409-12 (Oct 1999) ISSN: 0026-4784 [Print] Italy
Vernacular TitleDeficit congenito del fattore XIII in gravidanza. Esposizione di un caso clinico.
PMID10638168 (Publication Type: Case Reports, Comparative Study, English Abstract, Journal Article)
Topics
  • Adult
  • Factor XIII Deficiency (congenital, diagnosis)
  • Female
  • Fetal Death (etiology)
  • Humans
  • Infant, Newborn
  • Male
  • Pregnancy
  • Pregnancy Complications, Hematologic (diagnosis)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: