Skip Navigation

Journal of Tropical Pediatrics 1997 43(2):71-74; doi:10.1093/tropej/43.2.71
© 1997 by Oxford University Press
This Article
Right arrow Full Text (PDF)
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (3)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Al-Nuaim, L.
Right arrow Articles by Warsy, A. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Al-Nuaim, L.
Right arrow Articles by Warsy, A. S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?


research-article

Sickle Cell and G-6-PD Deficiency Gene in Cord Blood Samples: Experience at King Khalid University Hospital, Riyadh

Lulu Al-Nuaim, MD*, Zeinab Abo Talib, MD*, Mohsen A. F. El-Hazmi, MD Ph.D**, and Arjumand S. Warsy***

*Department of Obstetrics & Gynaecology, College of Medicine & King Khalid University Hospital Riyadh, Saudi Arabia
**Department of Medicine Biochemistry & W.H.O. Collaborating Centre for Haemoglobinopathies, Thalassaemias and Enzymopathies, College of Medicine & King Khalid University Hospital Riyadh, Saudi Arabia
***Department of Biochemistry, College of Science, Sciences and Medical Studies, Department of Women Students, King Saud University Riyadh, Saudi Arabia

Address for correspondence: Prof. Dr Mohsen A. F. El-Hazmi, Department of Medical Biochemistry & W.H.O. Collaborating Centre for Haemoglobinopathies, Thalassaemias and Enzymopathies, College of Medicine & King Khalid University Hospital, P.O. Box 2925, Riyadh 11461, Saudi Arabia

Cord blood samples (1039) collected at King Khalid University Hospital were analysed for abnormal haemoglobins using electrophoresis at alkaline and acid pH, for glucose-6-phosphate dehydrogenase (G-6-PD) deficiency using spectrophotometric method and for G-6-PD phenotypes using electrophoresis and specific staining.

Only two samples showed the presence of Hb AS and no case of sickle cell anaemia was identified. The Hb S gene frequency was 0.00096. This was the lowest frequency identified so far in different regions of Saudi Arabia. The frequency of G-6-PD deficiency was calculated separately in the males and females, and was found to be 3.605 per cent in the males and 0.195 per cent in the females. Phenotyping showed the presence of G-6-PD-B+ as the normal enzyme at a frequency of 0.943 in both males and females and G-6-PD-A+ at a frequency of 0.0208 in males and 0.0059 in females. The deficient variant was mainly G-6-PD-Mediterranean which occurred at a frequency of 0.0341 and 0.0019 in males and females, respectively. Only one case of G-6-PD-A was identified in the males giving a frequency of 0.0019.

This is the first report of Hb S and G-6-PD deficiency genes in cord blood samples in Riyadh, Comparison of the results in Riyadh with values reported elsewhere showed that Riyadh had the lowest frequency of both Hb S and G-6-PD deficiency gene.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.