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A Case of Congenital Pelger-Huet Anomaly

The Ewha Medical Journal 1996;19(4):533-538. Published online: July 24, 2015

Department of Clinical Pathology, College of Medicine, Ewha Womans University, Korea.

*Department of Pediatrics, College of Medicine, Ewha Womans University, Korea.

Copyright © 1996. Ewha Womans University School of Medicine

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • Congenital Pelger-Huët anomaly is an autosomal dominant disorder affection leukocyte differentiation manifested by the presence of unsegmented of bilobed nuclei with increased condensation, but it is generally assumed that it has no clinical effects. We observed a case of congenital Pelger-Huët anomaly in 9 year-old boy. He was admitted to Ewha Womans University Hospital due to fever and diagnosed as viral infection of upper respiratory tract. On routine peripheral blood examination, we found majority of the neutrophils had uni-or bilobed nuclei. In familial examination, his mother & brother have had Pelger-Huët anomaly without any significant symptoms. On neutrophil function test, moderate defect of chemotaxis was noted.

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      Ihwa Ŭidae chi. 1996;19(4):533-538.   Published online July 24, 2015
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