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

Nazli Dilay Gultekin1, Fatma Hilal Yilmaz2, Huseyin Tokgoz3

  • 1Department of Neonatology, Necmettin Erbakan University Meram Medical Faculthy, Konya, Turkey. Correspondence to: Dr Nazli Dilay Gültekin, Department of Neonatology, Necmettin Erbakan University Meram Medical Faculthy, Konya, Turkey. dilayyenihan@hotmail.com.

Indian Pediatrics
|March 2, 2019
PubMed
Abstract

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