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Case Reports

Homozygous Form of the Pelger-Huët Leukocyte Anomaly in Man

Aznar J. · Vaya A.

Author affiliations

Department of Clinical Pathology, Ciudad Sanitaria ‘La Fe’, Valencia, Spain

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Acta Haematol 1981;66:59–62

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Article / Publication Details

First-Page Preview
Abstract of Case Reports

Received: October 22, 1980
Accepted: January 19, 1981
Published online: February 26, 2009
Issue release date: 1981

Number of Print Pages: 4
Number of Figures: 0
Number of Tables: 0

ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)

For additional information: http://www.karger.com/AHA

Abstract

A report on a new case of Pelger-Huët (PH) leukocyte anomaly in the homozygous form in an 18-month-old girl is presented. Clinically, the proband shows no special symptoms dependent on the leukocyte anomaly, but polydactyly affects both hands (six fingers on one hand) and feet (six toes on both feet). Her pedigree reveals the existence of three couples in which both husband and wife are heterozygous carriers of the PH anomaly. Study of the family lineage suggests that transmission of the leukocyte anomaly is prevailingly dominant in nature with complete penetration and variable expression.

© 1981 S. Karger AG, Basel


Article / Publication Details

First-Page Preview
Abstract of Case Reports

Received: October 22, 1980
Accepted: January 19, 1981
Published online: February 26, 2009
Issue release date: 1981

Number of Print Pages: 4
Number of Figures: 0
Number of Tables: 0

ISSN: 0001-5792 (Print)
eISSN: 1421-9662 (Online)

For additional information: http://www.karger.com/AHA


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