Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations

Author:

Gultekin Nazli Dilay,Yilmaz Fatma Hilal,Tokgoz Huseyin,Tarakci Nuriye,Caliskan Umran

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference10 articles.

1. George JN, Caen JP, Nurden AT. Glanzmann thrombasthenia: the spectrum of clinical disease. Blood. 1990;75:1383–95.

2. McGuinn C, Bussell JB. Disorders of Platelets. In: Lanzkowsky P, Lipton J, Fish J, editors. Manual of Pediatric Hematology and Oncology. 6th ed. London: Academic Press;2016. P. 262–301.

3. Coller BS, French DL. Hereditary Qualitative Platelet Disorders. In: Beutler E, Lichtman MA, Coller BS, Kipps TJ, Seligsohn U, editors. Williams’ Hematology. 6th ed. New York: McGraw–Hill Co;2001. P. 1551–60.

4. Nurden AT, Didry D, Kieffer N, McEver RP. Residual amounts of glycoproteins IIb and IIIa may be present in the platelets of most patients with Glanzmann’s thrombasthenia. Blood. 1985;65:1021–4.

5. Nurden AT, Pillois X, Nurden P. Understanding the genetic basis of Glanzmann thrombasthenia: Implications for treatment. Exp Rev Hematol. 2012;5:487–503.

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