Abstract
We describe four children with a novel primary immunodeficiency consisting of specific natural-killer (NK) cell deficiency and susceptibility to viral diseases. One child developed an Epstein-Barr virus-driven lymphoproliferative disorder; two others developed severe respiratory illnesses of probable viral etiology. The four patients are related and belong to a large inbred kindred of Irish nomadic descent, which suggests autosomal recessive inheritance of this defect. A genomewide scan identified a single 12-Mb region on chromosome 8p11.23-q11.21 that was linked to this immunodeficiency (maximum LOD score 4.51). The mapping of the disease-causing genomic region paves the way for the identification of a novel pathway governing NK cell differentiation in humans. © 2006 by The American Society of Human Genetics. All rights reserved.
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CITATION STYLE
Eidenschenk, C., Dunne, J., Jouanguy, E., Fourlinnie, C., Gineau, L., Bacq, D., … Feighery, C. (2006). A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8. American Journal of Human Genetics, 78(4), 721–727. https://doi.org/10.1086/503269
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