Clinical, Laboratory and Molecular Approach to Ten Children with Congenital Neutropenia
Articles > Article · 2016
Authors: Neslihan KARACA, Güzide AKSU, Nesrin GULEZ, Elif AZARSIZ, Ramazan Kaan KAVAKLI, Christoph KLEIN, Necil KÜTÜKÇÜLER
JOURNAL OF PEDIATRIC RESEARCH, Journal Indexed in SCI Expanded, International, 2016, vol 3, pp 7-12
DOI: 10.4274/jpr.19480
Summary
Aim: Severe congenital neutropenia is a rare immunodeficiency disease characterized by lack of mature neutrophils. We evaluated the association between the molecular, clinical and laboratory findings together with genotype-phenotype relationship in 10 patients with neutropenia.