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Up to: Leukocyte disorder · Autosomal dominant disease · Laminopathy
Pelger-Huet anomaly
An autosomal dominant inherited condition caused by mutations in the lamin B receptor gene. It is characterized by defects in the neutrophil lobulation, resulting in the presence of dumbbell-shaped neutrophils with bilobed nuclei in the peripheral blood smear.
This condition has no sub-types.