Pelger-Huet anomaly in an infant with multiple congenital anomalies.

Published

Journal Article

We report a new case of Pelger-Huet anomaly (PHA) evident from the first day of life in an infant with multiple congenital anomalies suggestive of Fryn syndrome. The infant's parents are not affected by PHA, raising the possibility that the PHA resulted from a spontaneous mutation.

Full Text

Duke Authors

Cited Authors

  • Fishbein, JD; Falletta, JM

Published Date

  • November 1991

Published In

Volume / Issue

  • 38 / 3

Start / End Page

  • 240 - 242

PubMed ID

  • 1951327

Pubmed Central ID

  • 1951327

International Standard Serial Number (ISSN)

  • 0361-8609

Digital Object Identifier (DOI)

  • 10.1002/ajh.2830380318

Language

  • eng

Conference Location

  • United States