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Hematology

Pelger-Huët Anomaly

by clinicalsci

Pelger-Huët anomaly (PHA), also known as true or congenital PHA, is an autosomal dominant condition marked by reduced nuclear segmentation (bilobed, unilobed) and a distinctive coarse chromatin clumping pattern that can involve any leukocyte, while morphologic differences are more noticeable in mature neutrophils. A mutation in the lamin β-receptor gene …

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Categories Hematology Tags Hematology, Leukocyte Disorder, Pelger-Huët Anomaly

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