Hemoglobin EE Disease: A Case Report

Hemoglobin EE Disease: A Case Report

Awad M. Al-Qahtani

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Mohamed S. M. Khalil

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Essam M. Ahmed

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α Najran University

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References

15 Cites in Article

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Ross Hardison,David Chui,Belinda Giardine,Cathy Riemer,George Patrinos,Nicholas Anagnou,Webb Miller,Henri Wajcman (2002). HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server.
N Yedla,M Kuchay,A Mithal (2015). Hemoglobin E disease and glycosylated hemoglobin.
N Olivieri,Z Pakbaz,E Vichinsky (2011). Hb E/beta-thalassaemia: a common & clinically diverse disorder.
E Kohne (2011). Hemoglobinopathies: clinical manifestations, diagnosis, and treatment.
E Katsanis,K H Luke,E Hsu,J Yates (1987). Hemoglobin E: a common hemoglobinopathy among children of Southeast Asian origin.
Little R R,W Roberts (2009). A review of variant hemoglobins interfering with hemoglobin A1c measurement.
David Weatherall (2008). Hemoglobinopathies Worldwide: Present and Future.
R Gibbons,Higgs D R,N Olivieri,W Wood (2001). The β and δβ Thalassaemias in Association with Structural Haemoglobin Variants.
S1 Fucharoen,D Weatherall (2012). The Hemoglobin E Thalassemias.
Suthat Fucharoen,Phairawh Ketvichit,Pensri Pootrakul,Noppadol Siritanaratkul,Anong Piankijagum,Prawase Wasi (2000). Clinical Manifestation of β-Thalassemia/Hemoglobin E Disease.
J Acquaye,A Omer,K Ganeshaguru,S Sejeny,A Hoffbrand (1985). Non-benign sickle cell anaemia in western Saudi Arabia.
Ziad Memish,Mohammad Saeedi (2011). Six-Year Outcome of the National Premarital Screening and Genetic Counseling Program for Sickle Cell Disease and β-Thalassemia in Saudi Arabia.
D Weatherall,J Clegg (2001). Inherited haemoglobin disorders: an increasing global health problem.
D Rees,J B Clegg,D Weatherall (1998). Is Hemoglobin Instability Important in the Interaction Between Hemoglobin E and β Thalassemia?.
Nagel R L,M Fabry,M Steinberg (2003). The paradox of hemoglobin SC disease.

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Funding

No external funding was declared for this work.

Conflict of Interest

The authors declare no conflict of interest.

Ethical Approval

No ethics committee approval was required for this article type.

Data Availability

Not applicable for this article.

How to Cite This Article

Awad M. Al-Qahtani. 2019. \u201cHemoglobin EE Disease: A Case Report\u201d. Global Journal of Medical Research - C: Microbiology & Pathology GJMR-C Volume 19 (GJMR Volume 19 Issue C2): .

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GJMR Volume 19 Issue C2
Pg. 11- 14

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Journal Specifications

Crossref Journal DOI 10.17406/gjmra

Print ISSN 0975-5888

e-ISSN 2249-4618

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Classification

GJMR-C Classification: NLMC Code: WH 190

Submission ReceivedDecember 12, 2018
Peer Review Double Blind
Handling Editor
Accepted January 2, 2019
Published January 15, 2019

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v1.2

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December 14, 2019

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