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Case Report

Human Hemoglobin G-Makassar Variant Masquerading as Sickle Cell Anemia

by
Ahmad Sabry Mohamad
1,*,
Roszymah Hamzah
2,
Veena Selvaratnam
2,
Subramanian Yegapan
2 and
Jameela Sathar
2
1
Medical Engineering Section, Universiti Kuala Lumpur—British Malaysian Institute, Gombak 53100, Selangor, Malaysia
2
Hematology Department, Ampang Hospital, Ampang 68000, Selangor, Malaysia
*
Author to whom correspondence should be addressed.
Hematol. Rep. 2018, 10(3), 7210; https://doi.org/10.4081/hr.2018.7210
Submission received: 4 May 2018 / Revised: 11 July 2018 / Accepted: 31 July 2018 / Published: 24 September 2018

Abstract

Human hemoglobin of G-Makassar variant has been reported very rarely with Beta Thalassemia. In year 1969 Hb G-Makassar was first identified in Makassar, Sulawesi (Celebes), Republic of Indonesia. The disease was first published in 1969 and 33 years later it has been reported at a family of Thailand origin. We report a 45-year-old Malay man who was investigated for anemia and thrombocytopenia then diagnosed with Hb G-Makassar. This finding describes as a new Hemoglobin G-Makassar discovered in Malaysia after 14 years diagnosed in Thailand.
Keywords: hemoglobin G-Makassar; electrophoresis; beta thalassemia; DNA analysis; sickle cell disease hemoglobin G-Makassar; electrophoresis; beta thalassemia; DNA analysis; sickle cell disease

Share and Cite

MDPI and ACS Style

Mohamad, A.S.; Hamzah, R.; Selvaratnam, V.; Yegapan, S.; Sathar, J. Human Hemoglobin G-Makassar Variant Masquerading as Sickle Cell Anemia. Hematol. Rep. 2018, 10, 7210. https://doi.org/10.4081/hr.2018.7210

AMA Style

Mohamad AS, Hamzah R, Selvaratnam V, Yegapan S, Sathar J. Human Hemoglobin G-Makassar Variant Masquerading as Sickle Cell Anemia. Hematology Reports. 2018; 10(3):7210. https://doi.org/10.4081/hr.2018.7210

Chicago/Turabian Style

Mohamad, Ahmad Sabry, Roszymah Hamzah, Veena Selvaratnam, Subramanian Yegapan, and Jameela Sathar. 2018. "Human Hemoglobin G-Makassar Variant Masquerading as Sickle Cell Anemia" Hematology Reports 10, no. 3: 7210. https://doi.org/10.4081/hr.2018.7210

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