2003Pediatric Hematology and OncologyRequires access

Use of Recombinant Factor VIIa for Bleeding in Children with Glanzmann Thrombasthenia

Kudret Çağlar, Ahmet Çetinkaya, Selin Aytaç, Fatma Gümrük, Aytemiz Gürgey

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Abstract

Glanzmann thrombasthenia is a very rare inherited platelet function disorder in which bleeding may be extremely difficult to stop. Recombinant factor VIIa is one of the alternative treatments for bleeding. The authors report here their experience with the use of factor VIIa, which may be useful for arresting bleeding in Glazmann thrombasthenia.

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What this paper is about

Glanzmann thrombasthenia is a very rare inherited platelet function disorder in which bleeding may be extremely difficult to stop. Recombinant factor VIIa is one of the alternative treatments for bleeding. The authors report here their experience with the use of factor VIIa, which may be useful for arresting bleeding in Glazmann thrombasthenia.

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Available abstract

Glanzmann thrombasthenia is a very rare inherited platelet function disorder in which bleeding may be extremely difficult to stop. Recombinant factor VIIa is one of the alternative treatments for bleeding. The authors report here their experience with the use of factor VIIa, which may be useful for arresting bleeding in Glazmann thrombasthenia.

Key concepts: Thrombasthenia, Medicine, Glanzmann's thrombasthenia, Recombinant factor VIIa, Factor VIIa, Platelet, Recombinant DNA, Surgery

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Use of Recombinant Factor VIIa for Bleeding in Children with Glanzmann Thrombasthenia — Research Paper | ScholarLens