Multiple cerebral emboli in a homozygous $beta$-thalassaemia patient due to factor V 1299 (His-Arg) 4070 A-G mutation

We report a patient with cerebral thromboembolic episode triggered by a minor blood group incompatibility in which the underlying defect of factor V 1299 (His-Arg) was detected three years after his death.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Thromboembolic episodes are quite rare in beta thalassemia major patients although there is a tendency for thrombosis in haemolytic anaemias.

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Temel Bulgular & Veri:Thromboembolic episodes are quite rare in beta thalassemia major patients although there is a tendency for thrombosis in haemolytic anaemias.

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Sonuç & Katkı:We report a patient with cerebral thromboembolic episode triggered by a minor blood group incompatibility in which the underlying defect of factor V 1299 (His-Arg) was detected three years after his death.

🔬Tür:Araştırma Makalesi

📍Kapsam:Genişletilmiş Akademik Örneklem

⚙️Değişkenler:Alan Parametreleri

Abstract

Thromboembolic episodes are quite rare in beta thalassemia major patients although there is a tendency for thrombosis in haemolytic anaemias. We report a patient with cerebral thromboembolic episode triggered by a minor blood group incompatibility in which the underlying defect of factor V 1299 (His-Arg) was detected three years after his death.

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Bu Makaleye Atıf Yap

AKAR, N., CİN, Ş., DEDA, G., KEMAHLI, S., UYSAL, Z., YILMAZ, E., AKAR, E. (2022). Multiple cerebral emboli in a homozygous $beta$-thalassaemia patient due to factor V 1299 (His-Arg) 4070 A-G mutation. Turkish Journal of Hematology, Cilt: 17 - Sayı: 3, 133–136. https://ajindex.com/articles/607138

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Kaynakça (13)

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