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Pelger—Huet anomaly in an infant with multiple congenital anomalies
Author(s) -
Fishbein Julie D.,
Falletta John M.
Publication year - 1991
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.2830380318
Subject(s) - anomaly (physics) , medicine , pediatrics , physics , condensed matter physics
Abstract 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.