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

Introduction Glanzmann thrombasthenia is a rare congenital platelet dysfunction. Case characteristics A 2-day-old male neonate delivered at 35 weeks’ gestation was referred with extensive bruising and jaundice. His elder sibling had Glanzmann thrombasthenia, and his mother had thrombophilic risk fac...

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Veröffentlicht in:	Indian pediatrics 2019-02, Vol.56 (2), p.143-144
Hauptverfasser:	Gultekin, Nazli Dilay, Yilmaz, Fatma Hilal, Tokgoz, Huseyin, Tarakci, Nuriye, Caliskan, Umran
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Report Maternal and Child Health Medicine Medicine & Public Health Pediatric Surgery Pediatrics
Online-Zugang:	Volltext
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