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Journals / Ege Pediatri Bülteni / 2007 / Cilt: 14 - Sayı: 2

Congenital factor VII deficiency (case report)

Konjenital faktör VII eksikliği (olgu sunumu)

Mehmet HELVACI
Pelin KÖŞGER
Münevver YILDIRIMER
Esra Arun ÖZER
Şervan ÖZALKAR
Pages
123–126
Publication Date
2022-10-17
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this paper, a neonatal case of factor VII deficiency died of intracranial hemorrhage is presented.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Factor VII deficiency is a rare autosomal recessive bleeding disorder.
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Key Findings & Data:Although prolonged prothrombin time with normal partial thromboplastin time is a sensitive finding for factor VII deficiency, definitive diagnosis is established by measuring plasma factor VII level.
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Conclusion & Impact:In this paper, a neonatal case of factor VII deficiency died of intracranial hemorrhage is presented.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Factor VII deficiency is a rare autosomal recessive bleeding disorder. Although prolonged prothrombin time with normal partial thromboplastin time is a sensitive finding for factor VII deficiency, definitive diagnosis is established by measuring plasma factor VII level. This disease may lead to death with serious bleeding in the neonatal and early infantile period. In this paper, a neonatal case of factor VII deficiency died of intracranial hemorrhage is presented.

Özet

Konjenital faktör VII eksikliği, otozomal ressesif kalıtılan nadir bir kanama bozukluğudur. Koagulasyon testlerinde protrombin zamanının (PT) uzun, parsiyel tromboplastin zamanının (PTT) normal olması bu hastalığı düşündürmekle birlikte, kesin tanı plazma faktör VII seviyesinin ölçümü ile konulmaktadır. Yenidoğan ve erken süt çocukluğu döneminde ciddi kanamalara yol açarak yaşamı tehdit edebildiği bilinmektedir. Bu yazıda, intrakranyal kanama nedeni ile kaybedilen, yapılan tetkiklerinde faktör VII eksikliği saptanan bir yenidoğan olgusu sunulmaktadır.

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Cite This Article

HELVACI, M., KÖŞGER, P., YILDIRIMER, M., ÖZER, E. A., ÖZALKAR, Ş. (2022). Congenital factor VII deficiency (case report). Ege Pediatri Bülteni, Cilt: 14 - Sayı: 2, 123–126. https://ajindex.com/articles/495702

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References (7)

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