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Journals / Turkish Journal of Pediatrics / 2020 / Cilt: 62 - Sayı: 2

Congenital afibrinogenemia in a 4-year-old girl complicated with acute lymphoblastic leukemia

Alper OZCAN
Bahadır SAMUR
Şefika AKYOL
Arda ERDOGMUS
Turkan PATIROGLU
MUSA KARAKÜKCÜ
Ekrem ÜNAL
Pages
289–292
DOI
—
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AI Summary & Key Takeaways

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

This case aims to highlight therapeutic approaches for the management of afibrinogenemia patients with acute leukemia.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Congenital fibrinogen deficiency is one of the rare inherited coagulation disorders.
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Key Findings & Data:Congenital fibrinogen deficiency complicated with a hematological malignancy can be life threatening.
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Conclusion & Impact:This case aims to highlight therapeutic approaches for the management of afibrinogenemia patients with acute leukemia.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Background. Congenital fibrinogen deficiency is one of the rare inherited coagulation disorders. Congenital fibrinogen deficiency complicated with a hematological malignancy can be life threatening. Case. We present a four-year-old girl with congenital fibrinogen deficiency complicated with acute lymphoblastic leukemia. Conclusion. This case aims to highlight therapeutic approaches for the management of afibrinogenemia patients with acute leukemia.

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Cite This Article

OZCAN, A., SAMUR, B., AKYOL, Ş., ERDOGMUS, A., PATIROGLU, T., KARAKÜKCÜ, M., ÜNAL, E. (2020). Congenital afibrinogenemia in a 4-year-old girl complicated with acute lymphoblastic leukemia. Turkish Journal of Pediatrics, Cilt: 62 - Sayı: 2, 289–292. https://ajindex.com/articles/411850

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