Pelger-Huet anomaly

Pelger-Huet anomaly
ICD-10	D72.0
ICD-9	288.2
OMIM	169400
DiseasesDB	29515
eMedicine	ped/1753
MeSH	D010381

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Pelger-Huet anomaly is a blood laminopathy associated with the lamin B receptor. It is characterized by a white blood cell type known as a neutrophil whose nucleus is hyposegmented.

It is a genetic disorder with an autosomal dominant inheritance pattern. Heterozygotes are clinical normal although their neutrophils may be mistaken for immature cells which may cause mistreatment in a clinical setting. Homozygotes tend to have neutrophils with rounded nuclei that do have some functional problems.

Pelger-Huet anomaly has an autosomal dominant pattern of inheritance.