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KMID : 0366219890240020497
Korean Journal of Hematology
1989 Volume.24 No. 2 p.497 ~ p.500
A Case of Congenital Pelger-Hu t Anomaly of Leukocyte
ÁöÇö¿µ/Chi Hyun Young
±èÇöÅÂ/¹Ú¾ÖÀÚ/Hyoun Tae Kim/Ae Ja Park
Abstract
The Pelger-Hu t anomaly is a hereditary abnormality of granulocytes characterized by
failure of nuclear segmentation. A 21 year old man shows Pelter-Hu t anomaly on
routine CBC examination. His mother reveals Pelger-Hu t anomaly in his family,
without specific symptoms. The peripheral blood smears of these 2 members reveals
98-99% Pelter-Hu t anomaly in PMN. So the authors report 3rd case of congenital
Pelter-Hu t anomaly in Korea with brief review of literature.
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