Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)

Abstract

The Immunodeficiency, Centromeric region instability, Facial anomalies syndrome (ICF) is a rare autosomal recessive disease described in about 50 patients worldwide and characterized by immunodeficiency, although B cells are present, and by characteristic rearrangements in the vicinity of the centromeres (the juxtacentromeric heterochromatin) of chromosomes… (More)

Topics

Cite this paper

@article{Ehrlich2006ImmunodeficiencyCR, title={Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)}, author={Melanie Ehrlich and Kelly E Jackson and Corry M. R. Weemaes}, journal={Orphanet Journal of Rare Diseases}, year={2006}, volume={1}, pages={2 - 2} }