1744
Inherited bi-lobed neutrophil which is benign and associated with coarse nuclear chromatin and without functional defects.
Heterozygote expression of an autosomal dominant disorder found in 1 in 6000 births.
Pseudo Pelger-Huet anomaly reflects acquired changes seen in myelodysplastic disorders, myeloproliferative disease, acute leukemia, drugs, and rarely acute infections.