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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
We report a 21 days old, congenital hypofibrinogenemia case with cord bleeding.
📌 3 Key Takeaways
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Objective & Hypothesis:The genetic disorders causing decreased fibrinogen synthesis may be caused by heterozygous (hypofibrinogenemia) or homozygous (afibrinogenemia) deficiency.
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Key Findings & Data:Laboratory evaluation of the patient with hypofibrinogenemia reveals prolongation of thrombin time, partial thromboplastin time, prothrombin time and decreased fibrinogen level.
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Conclusion & Impact:We report a 21 days old, congenital hypofibrinogenemia case with cord bleeding.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Fetal kan · Afibrinogenemi · Süt çocuğu
Özet
The genetic disorders causing decreased fibrinogen synthesis may be caused by heterozygous (hypofibrinogenemia) or homozygous (afibrinogenemia) deficiency. The consequences of the disorders are gastrointestinal bleeding, cord bleeding, eccymoses, subcutaneous hematomas and hemarthroses especially due to traumatic delivery in the neonatal period. Laboratory evaluation of the patient with hypofibrinogenemia reveals prolongation of thrombin time, partial thromboplastin time, prothrombin time and decreased fibrinogen level. We report a 21 days old, congenital hypofibrinogenemia case with cord bleeding.
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Cite This Article
YAPICIOĞLU, H., NARLI, N., SATAR, M., ANTMEN, B. (2000). Congenital hypofibrinogenemia: A newborn infant with cord bleeding. Turkish Journal of Hematology, Cilt: 17 - Sayı: 4, 217–219. https://ajindex.com/articles/412964