Congenital Pelger-Huet anomaly in triplets.

Published

Journal Article

Congenital Pelger-Huet anomaly is an autosomal dominant disorder characterized by incomplete nuclear segmentation of granulocytes. The morphology of these mature but hyposegmented granulocytes may be confused with that of immature granulocytes (bands), thereby suggesting bacterial infection. We report the first known case of triplets with this condition, and emphasize the need to identify accurately this normal variant.

Full Text

Duke Authors

Cited Authors

  • Ware, R; Kurtzberg, J; Brazy, J; Falletta, JM

Published Date

  • March 1988

Published In

Volume / Issue

  • 27 / 3

Start / End Page

  • 226 - 227

PubMed ID

  • 3348208

Pubmed Central ID

  • 3348208

International Standard Serial Number (ISSN)

  • 0361-8609

Digital Object Identifier (DOI)

  • 10.1002/ajh.2830270316

Language

  • eng

Conference Location

  • United States