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KMID : 0366219900250010259
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Korean Journal of Hematology
1990 Volume.25 No. 1 p.259 ~ p.265
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Two Cases of Congenital Pelger-Huet Anomaly
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고창석/Chang Seok Koh
노순태/이종봉/김용민/김소연/조민구/이권전/Soon Tae Rho/Jong Bong Lee/Yong Min Kim/So Yon Kim/Min Koo Cho/Gwon Jun Lee
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Abstract
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Congenital Pelger-Huet anomaly is an autosomal dominant disorder of leukocytes
characterized by failure of nuclear segmentation without functional disturbance.
Recently the authors experienced two cases of congenital Pe1ger-Huet anomaly on
routine hematologic examination in a 42-year-old woman and a 21-year-old man. Seven
persons of her family and four persons of his family have congenital Pelger-Huet
anomaly.
So the authors report two cases with brief review of literature.
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