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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
Herein, we report a 1-month-old girl presented with high phenylalanine level in national newborn screening program for phenylketonuria; and subsequently diagnosed to have acute lymphoblastic leukemia.
📌 3 Key Takeaways
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Objective & Hypothesis:Infant leukemia is a very rare disease and consists of 5% of all childhood leukemias.
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Key Findings & Data:Infant leukemia usually presents with high leukocyte counts and numerous extra-hematological features including central nervous system and skin involvement.
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Conclusion & Impact:Herein, we report a 1-month-old girl presented with high phenylalanine level in national newborn screening program for phenylketonuria; and subsequently diagnosed to have acute lymphoblastic leukemia.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Özet
Infant leukemia is a very rare disease and consists of 5% of all childhood leukemias. Infant leukemia usually presents with high leukocyte counts and numerous extra-hematological features including central nervous system and skin involvement. Herein, we report a 1-month-old girl presented with high phenylalanine level in national newborn screening program for phenylketonuria; and subsequently diagnosed to have acute lymphoblastic leukemia.
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Cite This Article
BAJİN, İ. Y., YILDIZ, Y., AKIN, Ş., AYTAÇ, S., ÜNAL, Ş., KUŞKONMAZ, B., ÇETİN, M., SİVRİ, S., GÜMRÜK, F. (2019). Infant Acute Lymphoblastic Leukemia with Atypical Presentation. Acta Medica, Cilt: 50 - Sayı: 4, 57–59. https://ajindex.com/articles/143127