Pelger-huët anomaly first report from Jordan : a case report
Joint Authors
Shubaylat, Taysir
al-Qaddumi, Ayman A.
Hakuz, Basmah
Wuraykat, Abd al-Razzaq A.
Source
Journal of the Royal Medical Services
Issue
Vol. 13, Issue 2 (30 Dec. 2006)4 p.
Publisher
The Royal Medical Services Jordan Armed Forces
Publication Date
2006-12-30
Country of Publication
Jordan
No. of Pages
4
Main Subjects
Topics
Abstract EN
The Pelger-Huet anomaly is a benign hereditary autosomal condition that involves failure of normal segmentation of granulocytic nuclei.
Most nuclei are band-shaped or have two nuclei. Here is a report of a 29-year-old single Jordanian female with Pelger-Huet anomaly.
Her peripheral blood smear showed extreme hypolobulation of granulocytes with presence of giant platelets.
The same patient was found to have B-thalassemia intermedia.
Both parents were also found to have the Pelger-Huet anomaly.
American Psychological Association (APA)
al-Qaddumi, Ayman A.& Hakuz, Basmah& Wuraykat, Abd al-Razzaq A.& Shubaylat, Taysir. 2006. Pelger-huët anomaly first report from Jordan : a case report. Journal of the Royal Medical Services،Vol. 13, no. 2.
https://search.emarefa.net/detail/BIM-106263
Modern Language Association (MLA)
al-Qaddumi, Ayman A.…[et al.]. Pelger-huët anomaly first report from Jordan : a case report. Journal of the Royal Medical Services Vol. 13, no. 2 (Dec. 2006).
https://search.emarefa.net/detail/BIM-106263
American Medical Association (AMA)
al-Qaddumi, Ayman A.& Hakuz, Basmah& Wuraykat, Abd al-Razzaq A.& Shubaylat, Taysir. Pelger-huët anomaly first report from Jordan : a case report. Journal of the Royal Medical Services. 2006. Vol. 13, no. 2.
https://search.emarefa.net/detail/BIM-106263
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-106263
